Browse Device Recalls
139 FDA medical device safety recalls.
FDA Medical Device Recall Enforcement Database
Browse 139 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 139 FDA device recalls.
| Date | Product | Reason | Class | Firm |
|---|---|---|---|---|
| Sep 4, 2012 | Zimmer Inverse/Reverse Screw system, | Zimmer Inc., is initiating a correction to the patient labels of products manufactured before Mar... | Class II | Zimmer, Inc. |
| Sep 4, 2012 | MS-30 Shaft, Sterile, Rx | Zimmer Inc., is initiating a correction to the patient labels of products manufactured before Mar... | Class II | Zimmer, Inc. |
| Sep 4, 2012 | Anatomical Shoulder" Revision Humeral stem,7,9,12,14 and Anatomical Shoulder... | Zimmer Inc., is initiating a correction to the patient labels of products manufactured before Mar... | Class II | Zimmer, Inc. |
| Sep 4, 2012 | Biolox¿ delta Ceramic Femoral Head Rx only, sterile | Zimmer Inc., is initiating a correction to the patient labels of products manufactured before Mar... | Class II | Zimmer, Inc. |
| Sep 4, 2012 | Metasul¿ LDH¿ Head Rx Sterile | Zimmer Inc., is initiating a correction to the patient labels of products manufactured before Mar... | Class II | Zimmer, Inc. |
| Sep 4, 2012 | Anatomical Shoulder" Fracture Humeral Head | Zimmer Inc., is initiating a correction to the patient labels of products manufactured before Mar... | Class II | Zimmer, Inc. |
| Sep 4, 2012 | MS-30¿ Proximal positioner | Zimmer Inc., is initiating a correction to the patient labels of products manufactured before Mar... | Class II | Zimmer, Inc. |
| Sep 4, 2012 | CoCr Head, sterile, Rx | Zimmer Inc., is initiating a correction to the patient labels of products manufactured before Mar... | Class II | Zimmer, Inc. |
| Sep 4, 2012 | Wagner cone Prosthesis, uncemented, sterile, Rx | Zimmer Inc., is initiating a correction to the patient labels of products manufactured before Mar... | Class II | Zimmer, Inc. |
| Sep 4, 2012 | Wagner SL Revision Stem, uncemented Sterile | Zimmer Inc., is initiating a correction to the patient labels of products manufactured before Mar... | Class II | Zimmer, Inc. |
| Sep 4, 2012 | Alloclassic¿ SL-Offset Stem sterile, Rx | Zimmer Inc., is initiating a correction to the patient labels of products manufactured before Mar... | Class II | Zimmer, Inc. |
| Sep 4, 2012 | Sirus¿ intramedullary nail for tibia, cannulated ¿ | Zimmer Inc., is initiating a correction to the patient labels of products manufactured before Mar... | Class II | Zimmer, Inc. |
| Sep 4, 2012 | Dynesys¿ L.I.S. Stabilizing cord Rx, Sterile | Zimmer Inc., is initiating a correction to the patient labels of products manufactured before Mar... | Class II | Zimmer, Inc. |
| Sep 4, 2012 | NCB¿-PT lateral proximal 3 hole tibial plate | Zimmer Inc., is initiating a correction to the patient labels of products manufactured before Mar... | Class II | Zimmer, Inc. |
| Sep 4, 2012 | Dynesys¿ Universal spacer 6-45 | Zimmer Inc., is initiating a correction to the patient labels of products manufactured before Mar... | Class II | Zimmer, Inc. |
| Sep 4, 2012 | Dynesys¿ Set screw M6 | Zimmer Inc., is initiating a correction to the patient labels of products manufactured before Mar... | Class II | Zimmer, Inc. |
| Sep 4, 2012 | Metasul¿ Durom¿ Femoral component Sterile, Rx | Zimmer Inc., is initiating a correction to the patient labels of products manufactured before Mar... | Class II | Zimmer, Inc. |
| Sep 4, 2012 | NCB¿-PH Plate | Zimmer Inc., is initiating a correction to the patient labels of products manufactured before Mar... | Class II | Zimmer, Inc. |
| Sep 4, 2012 | Dynesys¿ HA Pedicle + set screw | Zimmer Inc., is initiating a correction to the patient labels of products manufactured before Mar... | Class II | Zimmer, Inc. |
| Sep 4, 2012 | Fitmore" Hip Stem | Zimmer Inc., is initiating a correction to the patient labels of products manufactured before Mar... | Class II | Zimmer, Inc. |
| Sep 4, 2012 | Kopf Adapter S Sterile, Rx | Zimmer Inc., is initiating a correction to the patient labels of products manufactured before Mar... | Class II | Zimmer, Inc. |
| Sep 4, 2012 | NCB¿ cancellous screw | Zimmer Inc., is initiating a correction to the patient labels of products manufactured before Mar... | Class II | Zimmer, Inc. |
| Sep 4, 2012 | Anatomical Shoulder" Humeral Head | Zimmer Inc., is initiating a correction to the patient labels of products manufactured before Mar... | Class II | Zimmer, Inc. |
| Sep 4, 2012 | Original M.E. Mueller" Low Profile Cup Sterile, Rx | Zimmer Inc., is initiating a correction to the patient labels of products manufactured before Mar... | Class II | Zimmer, Inc. |
| Sep 4, 2012 | CLS Stem | Zimmer Inc., is initiating a correction to the patient labels of products manufactured before Mar... | Class II | Zimmer, Inc. |
| Sep 4, 2012 | MS-30¿ Distal centralizer, cemented, sterile, Rx | Zimmer Inc., is initiating a correction to the patient labels of products manufactured before Mar... | Class II | Zimmer, Inc. |
| Sep 4, 2012 | Anatomical Shoulder" Humeral stem | Zimmer Inc., is initiating a correction to the patient labels of products manufactured before Mar... | Class II | Zimmer, Inc. |
| Sep 4, 2012 | MS-30¿ Stem | Zimmer Inc., is initiating a correction to the patient labels of products manufactured before Mar... | Class II | Zimmer, Inc. |
| Sep 4, 2012 | Dynesys¿ Revision + set screw | Zimmer Inc., is initiating a correction to the patient labels of products manufactured before Mar... | Class II | Zimmer, Inc. |
| Sep 4, 2012 | Anatomical Shoulder" Inverse/Reverse Glenoid Sterile, Rx | Zimmer Inc., is initiating a correction to the patient labels of products manufactured before Mar... | Class II | Zimmer, Inc. |
| Sep 4, 2012 | Anatomical Shoulder" Inverse Humeral Cup | Zimmer Inc., is initiating a correction to the patient labels of products manufactured before Mar... | Class II | Zimmer, Inc. |
| Sep 4, 2012 | zimmer Anatomical Shoulder Glenoid S, cemented, sterile; REF 01.04214.340 P... | Zimmer Inc., is initiating a correction to the patient labels of products manufactured before Mar... | Class II | Zimmer, Inc. |
| Sep 4, 2012 | Biolox¿ Option Ceramic Femoral Head System Rx, sterile | Zimmer Inc., is initiating a correction to the patient labels of products manufactured before Mar... | Class II | Zimmer, Inc. |
| Sep 4, 2012 | Anatomical Shoulder" Inverse/Reverse Humeral PE-Insert Sterile, Rx | Zimmer Inc., is initiating a correction to the patient labels of products manufactured before Mar... | Class II | Zimmer, Inc. |
| Sep 4, 2012 | Alloclassic SL Shaft | Zimmer Inc., is initiating a correction to the patient labels of products manufactured before Mar... | Class II | Zimmer, Inc. |
| Sep 4, 2012 | Anatomical Shoulder" Fracture Humeral stem | Zimmer Inc., is initiating a correction to the patient labels of products manufactured before Mar... | Class II | Zimmer, Inc. |
| Sep 4, 2012 | DTO" Implant | Zimmer Inc., is initiating a correction to the patient labels of products manufactured before Mar... | Class II | Zimmer, Inc. |
| Sep 4, 2012 | NCB¿ screw ¿ 4.0 self-tapping | Zimmer Inc., is initiating a correction to the patient labels of products manufactured before Mar... | Class II | Zimmer, Inc. |
| Sep 4, 2012 | Dynesys¿ Top-Loading System Cannulated Pedicle + Set Screw | Zimmer Inc., is initiating a correction to the patient labels of products manufactured before Mar... | Class II | Zimmer, 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.