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Browse Device Recalls

4 FDA medical device safety recalls.

FDA Medical Device Recall Enforcement Database

Browse 4 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 4 FDA device recalls.

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DateProductReasonClassFirm
Jul 27, 2018 ZIMMER Oscillating Saw Blade -Cutting 75mm x 19mm x 1.00/1.27mm.intended for ... Mislabeled: Actual blade width is 19 mm but the label indicates a width of 25 mm. Class II Synvasive Technology Inc
Dec 8, 2015 Zimmer Oscillating Flat - TS ST Hub; 75mm x 19mm x 1.00/1.27mm; Synvasive... Two lots of oscillating saw blades incorrectly identify the blade cutting width as 25mm instead ... Class II Synvasive Technology Inc
Apr 2, 2013 Product is distributed by Zimmer (Warsaw, Indiana)/Synvasive Technology, Inc.... Various reciprocating and oscillating saw blades were incorrectly labeled. The labeling errors in... Class II Synvasive Technology Inc
Mar 14, 2013 The Oxford Partial Knee; Oxford Knee Resection Procedure 3 Pack CEMENTED For... Biomet part # 506076, lot 928182 was received from Synvasive Technology containing the incorrect ... Class II Synvasive Technology 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.