Browse Device Recalls
155 FDA medical device safety recalls.
FDA Medical Device Recall Enforcement Database
Browse 155 FDA medical device recall enforcement actions. Each entry includes the device description, reason for recall, classification (Class I through III based on severity), recalling firm, and distribution details. Use the filters below to search by year, classification, state, or keyword.
Medical Device Recalls
Browse 155 FDA device recalls.
| Date | Product | Reason | Class | Firm |
|---|---|---|---|---|
| Nov 18, 2013 | SIGMA¿ LCS¿ HIGH PERFORMANCE" MBT PUNCH NONCEMENTED Size 4-7 HP M.B.T. Kee... | DePuy Orthopaedics, Inc. is issuing a voluntary device correction of the HP M.B.T. Keel Punch Kne... | Class II | DePuy Orthopaedics, Inc. |
| Sep 16, 2013 | SmartSet¿ Endurance GMV, Gentamicin, REF 3105-040, Medium Viscosity Antibiot... | The SmartSet¿ GMV Endurance Gentamicin Bone Cement, product ref: number 3105-040 is intended for ... | Class II | DePuy Orthopaedics, Inc. |
| Jul 11, 2013 | LPS Lower Extremity Dovetail Intercalary component. Intended for use in re... | The LPS Lower Extremity Dovetail Intercalary component has the potential for fracture of the fema... | Class I | DePuy Orthopaedics, Inc. |
| May 8, 2013 | DePuy LifeLiner Stick & Cut Resistant Gloves Rt, Lg Part No. 5200-68-000 ... | LifeLiner Stick and Cut Resistant Gloves are being recalled because cases and individual glove pa... | Class III | DePuy Orthopaedics, Inc. |
| May 3, 2013 | DePuy Glenosphere orientation guide Product Usage: The glenosphere o... | The Glenosphere Orientation Guide Instrument Used with the Delta XTEND Reverse Shoulder is being ... | Class II | DePuy Orthopaedics, Inc. |
| Feb 25, 2013 | ReClaim Reamer Extension; Product code 2975-00-500, used with Reclaim Modular... | The tabs on the reamer extension device have broken. DePuy is notifying surgeons of the issue to ... | Class II | DePuy Orthopaedics, Inc. |
| Feb 5, 2013 | Specialist 2 IM Rod, Non-Sterile and associated Surgical Techniques: Sigma ... | Potential for the IM rod to break, leaving fragments in the patient. Surgical Techniques guidance... | Class II | DePuy Orthopaedics, Inc. |
| Jan 4, 2013 | LPS Diaphyseal Sleeves Product Usage: The LPS Diaphyseal Sleeves are used... | DePuy Orthopaedics is initiating a voluntary recall of the LPS Diaphyseal sleeve because the prod... | Class I | DePuy Orthopaedics, Inc. |
| Jan 4, 2013 | LPS Diaphyseal Sleeves Product Usage: The LPS Diaphyseal Sleeves are used... | DePuy Orthopaedics is initiating a voluntary recall of the LPS Diaphyseal sleeve because the prod... | Class I | DePuy Orthopaedics, Inc. |
| Jan 4, 2013 | LPS Diaphyseal Sleeves Product Usage: The LPS Diaphyseal Sleeves are used... | DePuy Orthopaedics is initiating a voluntary recall of the LPS Diaphyseal sleeve because the prod... | Class I | DePuy Orthopaedics, Inc. |
| Jan 4, 2013 | LPS Diaphyseal Sleeves Product Usage: The LPS Diaphyseal Sleeves are used... | DePuy Orthopaedics is initiating a voluntary recall of the LPS Diaphyseal sleeve because the prod... | Class I | DePuy Orthopaedics, Inc. |
| Dec 3, 2012 | SOL SYS 8IN CALCAR SZ12 Packaging: Product is packed within a poly protect... | An Engineering Analysis has determined the Solution Calcar Stem has the potential to result in im... | Class II | DePuy Orthopaedics, Inc. |
| Dec 3, 2012 | SOL SYS L 9IN CALC 2.25/16.5 Packaging: Product is packed within a poly pr... | An Engineering Analysis has determined the Solution Calcar Stem has the potential to result in im... | Class II | DePuy Orthopaedics, Inc. |
| Dec 3, 2012 | SOL SYS F 9 CALC L 13.5MM LG Packaging: Product is packed within a poly pr... | An Engineering Analysis has determined the Solution Calcar Stem has the potential to result in im... | Class II | DePuy Orthopaedics, Inc. |
| Dec 3, 2012 | SOL SYS R 9IN CALC 2.25/22.5 Packaging: Product is packed within a poly pr... | An Engineering Analysis has determined the Solution Calcar Stem has the potential to result in im... | Class II | DePuy Orthopaedics, Inc. |
| Dec 3, 2012 | SOL SYS L 9IN CALC 2.25/18 Packaging: Product is packed within a poly prot... | An Engineering Analysis has determined the Solution Calcar Stem has the potential to result in im... | Class II | DePuy Orthopaedics, Inc. |
| Dec 3, 2012 | SOL SYS L 9IN CALC 2.25/21 Packaging: Product is packed within a poly prot... | An Engineering Analysis has determined the Solution Calcar Stem has the potential to result in im... | Class II | DePuy Orthopaedics, Inc. |
| Dec 3, 2012 | SOL SYS 8IN CALC 1.5/15.0 Packaging: Product is packed within a poly prote... | An Engineering Analysis has determined the Solution Calcar Stem has the potential to result in im... | Class II | DePuy Orthopaedics, Inc. |
| Dec 3, 2012 | SOL SYS 8IN CALC 1.5/16.5 Packaging: Product is packed within a poly prote... | An Engineering Analysis has determined the Solution Calcar Stem has the potential to result in im... | Class II | DePuy Orthopaedics, Inc. |
| Dec 3, 2012 | SOL SYS R 9IN CALC 2.25/15.0 Packaging: Product is packed within a poly pr... | An Engineering Analysis has determined the Solution Calcar Stem has the potential to result in im... | Class II | DePuy Orthopaedics, Inc. |
| Dec 3, 2012 | SOL SYS F 9 CALC L 13.5MM LG Packaging: Product is packed within a poly pr... | An Engineering Analysis has determined the Solution Calcar Stem has the potential to result in im... | Class II | DePuy Orthopaedics, Inc. |
| Dec 3, 2012 | SOL SYS L 9IN CALC 2.25/22.5 Packaging: Product is packed within a poly pr... | An Engineering Analysis has determined the Solution Calcar Stem has the potential to result in im... | Class II | DePuy Orthopaedics, Inc. |
| Dec 3, 2012 | SOL SYS R 9IN CALC 2.25/19.5 Packaging: Product is packed within a poly pr... | An Engineering Analysis has determined the Solution Calcar Stem has the potential to result in im... | Class II | DePuy Orthopaedics, Inc. |
| Dec 3, 2012 | SOL SYS R 9IN CALC 2.25/21 Packaging: Product is packed within a poly prot... | An Engineering Analysis has determined the Solution Calcar Stem has the potential to result in im... | Class II | DePuy Orthopaedics, Inc. |
| Dec 3, 2012 | SOL SYS R 9IN CALC 2.25/18 Packaging: Product is packed within a poly prot... | An Engineering Analysis has determined the Solution Calcar Stem has the potential to result in im... | Class II | DePuy Orthopaedics, Inc. |
| Dec 3, 2012 | SOL SYS F 8 CALC 13.5MM LG Packaging: Product is packed within a poly prot... | An Engineering Analysis has determined the Solution Calcar Stem has the potential to result in im... | Class II | DePuy Orthopaedics, Inc. |
| Dec 3, 2012 | SOL SYS L 9IN CALC 2.25/19.5 Packaging: Product is packed within a poly pr... | An Engineering Analysis has determined the Solution Calcar Stem has the potential to result in im... | Class II | DePuy Orthopaedics, Inc. |
| Dec 3, 2012 | SOL SYS 8IN CALC 1.5/19.5 Packaging: Product is packed within a poly prote... | An Engineering Analysis has determined the Solution Calcar Stem has the potential to result in im... | Class II | DePuy Orthopaedics, Inc. |
| Dec 3, 2012 | SOL SYS R 9IN CALC 2.25/16.5 Packaging: Product is packed within a poly pr... | An Engineering Analysis has determined the Solution Calcar Stem has the potential to result in im... | Class II | DePuy Orthopaedics, Inc. |
| Dec 3, 2012 | SOL SYS L 9IN CALC 2.25/15.0 Packaging: Product is packed within a poly pr... | An Engineering Analysis has determined the Solution Calcar Stem has the potential to result in im... | Class II | DePuy Orthopaedics, Inc. |
| Dec 3, 2012 | SOL SYS 8IN CALC 1.5/18.0 Packaging: Product is packed within a poly prote... | An Engineering Analysis has determined the Solution Calcar Stem has the potential to result in im... | Class II | DePuy Orthopaedics, Inc. |
| Nov 28, 2012 | Pinnacle Cancellous Screw Packaging: Product is housed within a polyuretha... | DePuy Orthopaedics, Inc. is issuing a voluntary recall of ten lots of the Pinnacle¿ Cancellous Sc... | Class II | DePuy Orthopaedics, Inc. |
| Aug 22, 2012 | S-Rom¿ Total Hip System Poly Liner Packaging: The insert is placed into ... | Orthopaedics, Inc. (DePuy) is issuing a voluntary recall of four lots of the S-ROM" liner becaus... | Class II | DePuy Orthopaedics, Inc. |
| Jul 31, 2012 | DePuy Custom Implant Devices Packaging: Packaging was not standardized o... | In connection with a Warning Letter received from the U.S. Food & Drug Administration on December... | Class II | DePuy Orthopaedics, Inc. |
| Jul 24, 2012 | Altrx" Altralinked" Polyethylene liners Description: An acetabular liner i... | In the recalled lot, the products were not machined according to the production router, a size 52... | Class II | DePuy Orthopaedics, Inc. |
| May 16, 2012 | LUSTER HIP SZ 2 Packaging: The product was packaged within inner and outer... | DePuy Orthopaedics, Inc. is issuing a Field Safety Notice for the LUSTER Cemented Polished Femora... | Class II | DePuy Orthopaedics, Inc. |
| May 16, 2012 | ULTIMA*LX STM,POL 10/12TAP/3M Packaging: The product was packaged within i... | DePuy Orthopaedics, Inc. is issuing a Field Safety Notice for the LUSTER Cemented Polished Femora... | Class II | DePuy Orthopaedics, Inc. |
| May 16, 2012 | LUSTER HIP SZ 8 Packaging: The product was packaged within inner and outer... | DePuy Orthopaedics, Inc. is issuing a Field Safety Notice for the LUSTER Cemented Polished Femora... | Class II | DePuy Orthopaedics, Inc. |
| May 16, 2012 | ULTIMA*LX STM,POL 10/12TAP/SZ2 Packaging: The product was packaged within ... | DePuy Orthopaedics, Inc. is issuing a Field Safety Notice for the LUSTER Cemented Polished Femora... | Class II | DePuy Orthopaedics, Inc. |
| May 16, 2012 | ULTIMA*LX STM,POL 10/12TAP/SZ5 Packaging: The product was packaged within ... | DePuy Orthopaedics, Inc. is issuing a Field Safety Notice for the LUSTER Cemented Polished Femora... | Class II | DePuy Orthopaedics, Inc. |
| May 16, 2012 | LUSTER HIP SZ 4 Packaging: The product was packaged within inner and outer... | DePuy Orthopaedics, Inc. is issuing a Field Safety Notice for the LUSTER Cemented Polished Femora... | Class II | DePuy Orthopaedics, Inc. |
| May 16, 2012 | ULTIMA*LX STM,POL 10/12TAP/SZ3 Packaging: The product was packaged within ... | DePuy Orthopaedics, Inc. is issuing a Field Safety Notice for the LUSTER Cemented Polished Femora... | Class II | DePuy Orthopaedics, Inc. |
| May 16, 2012 | LUSTER HIP SZ 7 Packaging: The product was packaged within inner and outer... | DePuy Orthopaedics, Inc. is issuing a Field Safety Notice for the LUSTER Cemented Polished Femora... | Class II | DePuy Orthopaedics, Inc. |
| May 16, 2012 | LUSTER HIP SZ 6 Packaging: The product was packaged within inner and outer... | DePuy Orthopaedics, Inc. is issuing a Field Safety Notice for the LUSTER Cemented Polished Femora... | Class II | DePuy Orthopaedics, Inc. |
| May 16, 2012 | ULTIMA*LX STM,POL 10/12TAP/SZ4 Packaging: The product was packaged within ... | DePuy Orthopaedics, Inc. is issuing a Field Safety Notice for the LUSTER Cemented Polished Femora... | Class II | DePuy Orthopaedics, Inc. |
| May 16, 2012 | LUSTER HIP SZ 10 Packaging: The product was packaged within inner and oute... | DePuy Orthopaedics, Inc. is issuing a Field Safety Notice for the LUSTER Cemented Polished Femora... | Class II | DePuy Orthopaedics, Inc. |
| May 16, 2012 | ULTIMA*LX STM,POL 10/12TAP/1M Packaging: The product was packaged within i... | DePuy Orthopaedics, Inc. is issuing a Field Safety Notice for the LUSTER Cemented Polished Femora... | Class II | DePuy Orthopaedics, Inc. |
| May 16, 2012 | ULTIMA*LX STM,POL 10/12TAP/2M Packaging: The product was packaged within i... | DePuy Orthopaedics, Inc. is issuing a Field Safety Notice for the LUSTER Cemented Polished Femora... | Class II | DePuy Orthopaedics, Inc. |
| May 16, 2012 | ULTIMA*LX STM,POL 10/12TAP/4M Packaging: The product was packaged within i... | DePuy Orthopaedics, Inc. is issuing a Field Safety Notice for the LUSTER Cemented Polished Femora... | Class II | DePuy Orthopaedics, Inc. |
| May 16, 2012 | LUSTER HIP SZ 5 Packaging: The product was packaged within inner and outer... | DePuy Orthopaedics, Inc. is issuing a Field Safety Notice for the LUSTER Cemented Polished Femora... | Class II | DePuy Orthopaedics, Inc. |
Frequently Asked Questions
When a device safety issue is identified, the manufacturer or FDA initiates a recall. The FDA publishes an enforcement report detailing the device, the reason for the recall, and distribution. Healthcare facilities and providers are notified to check their inventory and take corrective action.
All types — from simple devices like blood glucose test strips and surgical gloves to complex devices like pacemakers, defibrillators, insulin pumps, hip implants, and ventilators. Software-driven devices are increasingly common in recalls due to bugs and cybersecurity vulnerabilities.
Use the search and filter tools on this page. Each recall entry includes the device description, model numbers, and distribution details so you can determine if your device is affected. Contact your healthcare provider if you find a match.