Browse Device Recalls
2,601 FDA medical device safety recalls.
FDA Medical Device Recall Enforcement Database
Browse 2,601 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 2,601 FDA device recalls in 2023.
| Date | Product | Reason | Class | Firm |
|---|---|---|---|---|
| Dec 1, 2023 | DUR PCA MTK REV INS LFT Intended for knee replacement Product Number:... | Product manufactured using UHMWPE raw material over 5 years of age has the potential for elevated... | Class II | Howmedica Osteonics Corp. |
| Dec 1, 2023 | SCORPIO RECESSED PATELLA- Intended for knee replacement Part Number: 3044-0030 | Product manufactured using UHMWPE raw material over 5 years of age has the potential for elevated... | Class II | Howmedica Osteonics Corp. |
| Dec 1, 2023 | LEFT SMALL-PCA MOD.REV.DUR.REV.INSERT Intended for knee replacement Part ... | Product manufactured using UHMWPE raw material over 5 years of age has the potential for elevated... | Class II | Howmedica Osteonics Corp. |
| Dec 1, 2023 | SCORPIO TS TIB INSERT -Intended for knee replacement Part Number: 72-4-0321 | Product manufactured using UHMWPE raw material over 5 years of age has the potential for elevated... | Class II | Howmedica Osteonics Corp. |
| Dec 1, 2023 | SCORPIO RECESSED PATELLA-Intended for knee repalcment Part Number: 3044-0032 | Product manufactured using UHMWPE raw material over 5 years of age has the potential for elevated... | Class II | Howmedica Osteonics Corp. |
| Dec 1, 2023 | SCORPIO RECESSED PATELLA- Intended for knee replacement Part Number: 3044-0028 | Product manufactured using UHMWPE raw material over 5 years of age has the potential for elevated... | Class II | Howmedica Osteonics Corp. |
| Dec 1, 2023 | SCORPIO RECESSED PATELLA- Intended for Knee Replacement Part Number: 3044-0026 | Product manufactured using UHMWPE raw material over 5 years of age has the potential for elevated... | Class II | Howmedica Osteonics Corp. |
| Dec 1, 2023 | DURATION A-P LIPPED TIB.INSERT-DURAC Intended for knee replacement ... | Product manufactured using UHMWPE raw material over 5 years of age has the potential for elevated... | Class II | Howmedica Osteonics Corp. |
| Dec 1, 2023 | SCORPIO U-DOME PATELLA -Intended for knee replacement Part Number: 7... | Product manufactured using UHMWPE raw material over 5 years of age has the potential for elevated... | Class II | Howmedica Osteonics Corp. |
| Dec 1, 2023 | SCORPIO TOTAL KNEE CONCENTRIC DOME PATELLA-SZ #7 -Intended for knee replaceme... | Product manufactured using UHMWPE raw material over 5 years of age has the potential for elevated... | Class II | Howmedica Osteonics Corp. |
| Dec 1, 2023 | SCORPIO TOTAL KNEE CONCENTRIC DOME PATELLA-SZ #9 -Intended for knee replaceme... | Product manufactured using UHMWPE raw material over 5 years of age has the potential for elevated... | Class II | Howmedica Osteonics Corp. |
| Dec 1, 2023 | SCORPIO U-DOME PATELLA -Intended for knee replacement Part Number: 73... | Product manufactured using UHMWPE raw material over 5 years of age has the potential for elevated... | Class II | Howmedica Osteonics Corp. |
| Dec 1, 2023 | SOLTIVE SuperPulsed Laser Fibers Model Numbers TFL-FBX150S, TFL-FBX200S, TFL... | Olympus identified inconsistencies in the Instructions for Use regarding cleaning the fiber tip a... | Class II | Olympus Corporation of the Americas |
| Dec 1, 2023 | LEFT SMALL-PCA MOD.REV.DUR.REV.INSERT Intended for knee replacement. ... | Product manufactured using UHMWPE raw material over 5 years of age has the potential for elevated... | Class II | Howmedica Osteonics Corp. |
| Dec 1, 2023 | SCORPIO TOTAL KNEE MEDIALIZED DOME PATELLA-SZ #11 -Intended for knee replacem... | Product manufactured using UHMWPE raw material over 5 years of age has the potential for elevated... | Class II | Howmedica Osteonics Corp. |
| Dec 1, 2023 | PS LIPPED TIBIAL INSERT ASSY DURACON Intended for knee replacement ... | Product manufactured using UHMWPE raw material over 5 years of age has the potential for elevated... | Class II | Howmedica Osteonics Corp. |
| Dec 1, 2023 | Vasoview Hemopro Endoscopic Vessel Harvesting System, model VH-3000-W . | Risk of polyimide particulate matter being present on the endoscopic harvesting vessel system. T... | Class II | Maquet Cardiovascular, LLC |
| Dec 1, 2023 | PRIMARY REV.TIB.INSERT-DURACON Intended for knee replacement. Prod... | Product manufactured using UHMWPE raw material over 5 years of age has the potential for elevated... | Class II | Howmedica Osteonics Corp. |
| Dec 1, 2023 | Scorpio-Flex Ttl Kn P-S Tib Brg Insrt Asy- -Intended for knee replacement ... | Product manufactured using UHMWPE raw material over 5 years of age has the potential for elevated... | Class II | Howmedica Osteonics Corp. |
| Nov 30, 2023 | Catalog No. 800 TRACHEOSTOMY CARE TRAY - STERILE -LATEX FREE | Firm is recalling all kits containing recalled lots of Nurse Assist Sterile 0.9% Normal Saline. N... | Class I | Busse Hospital Disposables, Inc. |
| Nov 30, 2023 | Spectral CT 7500, Software Version 5.0.0.X. Computed Tomography X-Ray System. | Multiple software issues that affect device functionality. | Class II | Philips North America Llc |
| Nov 30, 2023 | bkActiv Ultrasound System 2300, Model numbers 2300-56 and 2300-66. | An issue on the Dual Live Compare feature on the bkActiv system could result in a measurement error. | Class II | B-K Medical A/S |
| Nov 30, 2023 | GammaPod - Treatment Planning System-a component of the GammaPod Irradiation ... | Wrong structures imported into the GammaPod Treatment Planning System.-system allowed an RTSS gen... | Class II | Xcision Medical Systems, LLC |
| Nov 30, 2023 | Catalog No. 1443 DRESSING CHANGE TRAY / STERILE - LATEX FREE | Firm is recalling all kits containing recalled lots of Nurse Assist Sterile 0.9% Normal Saline. N... | Class I | Busse Hospital Disposables, Inc. |
| Nov 30, 2023 | Boston Scientific Model 3120 ZOOM LATITUDE Programmer/Recorder/Monitor (PRM) ... | The software application on the Programmer/Recorder/Monitor (PRM) for Implantable Pulse Generator... | Class II | Boston Scientific Corporation |
| Nov 30, 2023 | BrightView XCT, Gamma Camera, Product Code 882482 | While using Pre-Programmed Motion during an extrinsic quality assurance scan, a gap is created be... | Class II | Philips North America |
| Nov 30, 2023 | BrightView, Gamma Camera System, Product Code 882480. | While using Pre-Programmed Motion during an extrinsic quality assurance scan, a gap is created be... | Class II | Philips North America |
| Nov 30, 2023 | Catalog No. 9251R1, 9251R2, 9251R3 TRACHEOSTOMY CARE SET / STERILE - LATEX FREE | Firm is recalling all kits containing recalled lots of Nurse Assist Sterile 0.9% Normal Saline. N... | Class I | Busse Hospital Disposables, Inc. |
| Nov 30, 2023 | Link Patella Glide Resection Guide- For the implantation of the Endo-Model Kn... | Mislabeled: Angle and height of the device marked as L(large) corresponds to the small/medium dim... | Class II | Waldemar Link GmbH & Co. KG (Mfg Site) |
| Nov 30, 2023 | BrightView X, Gamma Camera, Product Code 882478 | While using Pre-Programmed Motion during an extrinsic quality assurance scan, a gap is created be... | Class II | Philips North America |
| Nov 30, 2023 | Omnipod 5 App (on compatible Android smartphones), Software Versions 1.1 - 1.... | The bolus calculator is not recording the decimal point if it is the first value entered when cha... | Class I | Insulet Corporation |
| Nov 29, 2023 | Custom procedural convenience kits and trays, Othopedic use, labeled as: a... | During an internal investigation, ACS identified that several components were "piggybacked" to AC... | Class II | American Contract Systems, Inc. |
| Nov 29, 2023 | Custom procedural convenience kits and trays, Ophthalmic use, labeled as: ... | During an internal investigation, ACS identified that several components were "piggybacked" to AC... | Class II | American Contract Systems, Inc. |
| Nov 29, 2023 | Custom procedural convenience kits and trays, anesthesia, labeled as: a) H... | During an internal investigation, ACS identified that several components were "piggybacked" to AC... | Class II | American Contract Systems, Inc. |
| Nov 29, 2023 | Custom procedural convenience kits and trays, urological, labeled as: a) U... | During an internal investigation, ACS identified that several components were "piggybacked" to AC... | Class II | American Contract Systems, Inc. |
| Nov 29, 2023 | Custom procedural convenience kits and trays, Obstetrical & Gynecological use... | During an internal investigation, ACS identified that several components were "piggybacked" to AC... | Class II | American Contract Systems, Inc. |
| Nov 29, 2023 | Custom procedural convenience kits and trays, general & plastic surgery, labe... | During an internal investigation, ACS identified that several components were "piggybacked" to AC... | Class II | American Contract Systems, Inc. |
| Nov 29, 2023 | Custom procedural convenience kits and trays, gastroenterological & urologica... | During an internal investigation, ACS identified that several components were "piggybacked" to AC... | Class II | American Contract Systems, Inc. |
| Nov 29, 2023 | Custom procedural convenience kits and trays, general hospital use, labeled a... | During an internal investigation, ACS identified that several components were "piggybacked" to AC... | Class II | American Contract Systems, Inc. |
| Nov 29, 2023 | Custom procedural convenience kits and trays, cardiac, labeled as: a) HEAR... | During an internal investigation, ACS identified that several components were "piggybacked" to AC... | Class II | American Contract Systems, Inc. |
| Nov 29, 2023 | Custom procedural convenience kits and trays, Obstetrical & Gynecological use... | During an internal investigation, ACS identified that several components were "piggybacked" to AC... | Class II | American Contract Systems, Inc. |
| Nov 29, 2023 | Custom procedural convenience kits and trays, Obstetrical & Gynecological use... | During an internal investigation, ACS identified that several components were "piggybacked" to AC... | Class II | American Contract Systems, Inc. |
| Nov 29, 2023 | Custom procedural convenience kits and trays, general hospital use, labeled a... | During an internal investigation, ACS identified that several components were "piggybacked" to AC... | Class II | American Contract Systems, Inc. |
| Nov 29, 2023 | Medline Gown Poly W/Breath Sleeves XL AAMIK Level 4 (Eclipse gown), REF SPT-2... | Surgical gowns were manufactured with the wrong sleeve. | Class II | MEDLINE INDUSTRIES, LP - Northfield |
| Nov 29, 2023 | Custom procedural convenience kits and trays, gastroenterological & urologica... | During an internal investigation, ACS identified that several components were "piggybacked" to AC... | Class II | American Contract Systems, Inc. |
| Nov 29, 2023 | Custom procedural convenience kits and trays, general & plastic surgery, labe... | During an internal investigation, ACS identified that several components were "piggybacked" to AC... | Class II | American Contract Systems, Inc. |
| Nov 29, 2023 | RX Series Copper (Cu) Assay Ref. Number CU2340 | Randox Laboratories have released an update to the Carryover Avoidance Technical Bulletin to deta... | Class II | Randox Laboratories Ltd. |
| Nov 29, 2023 | Custom procedural convenience kits and trays, cardiac, labeled as: a) CENT... | During an internal investigation, ACS identified that several components were "piggybacked" to AC... | Class II | American Contract Systems, Inc. |
| Nov 29, 2023 | Custom procedural convenience kits and trays, Obstetrical & Gynecological use... | During an internal investigation, ACS identified that several components were "piggybacked" to AC... | Class II | American Contract Systems, Inc. |
| Nov 29, 2023 | Custom procedural convenience kits and trays, ear, nose & throat, labeled as:... | During an internal investigation, ACS identified that several components were "piggybacked" to AC... | Class II | American Contract Systems, 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.