Product Recalls in Missouri
Product recalls affecting Missouri — including food, drugs, consumer products, medical devices, and vehicles distributed to Missouri. RecallDetector monitors distribution data from the FDA, USDA, CPSC, and NHTSA to show you which recalls are relevant to your area. 1,937 recalls have been distributed to Missouri in the last 12 months.
Showing 21621–21640 of 29,298 recalls
Recalled Item: IMPLANT Recalled by Zimmer Dental Inc Due to Information specific to the 3.7...
The Issue: Information specific to the 3.7 mmD and 4.1 mmD Trabecular Metal Zimmer...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: IMPLANT Recalled by Zimmer Dental Inc Due to Information specific to the 3.7...
The Issue: Information specific to the 3.7 mmD and 4.1 mmD Trabecular Metal Zimmer...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: IMPLANT Recalled by Zimmer Dental Inc Due to Information specific to the 3.7...
The Issue: Information specific to the 3.7 mmD and 4.1 mmD Trabecular Metal Zimmer...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: IMPLANT Recalled by Zimmer Dental Inc Due to Information specific to the 3.7...
The Issue: Information specific to the 3.7 mmD and 4.1 mmD Trabecular Metal Zimmer...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: IMPLANT Recalled by Zimmer Dental Inc Due to Information specific to the 3.7...
The Issue: Information specific to the 3.7 mmD and 4.1 mmD Trabecular Metal Zimmer...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: IMPLANT Recalled by Zimmer Dental Inc Due to Information specific to the 3.7...
The Issue: Information specific to the 3.7 mmD and 4.1 mmD Trabecular Metal Zimmer...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: IMPLANT Recalled by Zimmer Dental Inc Due to Information specific to the 3.7...
The Issue: Information specific to the 3.7 mmD and 4.1 mmD Trabecular Metal Zimmer...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: IMPLANT Recalled by Zimmer Dental Inc Due to Information specific to the 3.7...
The Issue: Information specific to the 3.7 mmD and 4.1 mmD Trabecular Metal Zimmer...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Cervical Spine Locking Plate (CSLP) System Recalled by Synthes (USA)...
The Issue: DePuy Synthes is initiating a Voluntary Medical Device Recall of lot #...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Oxford Partial Knee System Right Medial Tibial Trial Tray Size Recalled by...
The Issue: Zimmer Biomet is conducting a medical device field action for various...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: InVision-Plus and InVision-Plus Junior Needleless IV Connector Recalled by...
The Issue: Potential for the female luer component of the InVision-Plus IV connector to...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Oxford Partial Knee System Left Medial Tibial Trial Tray Size Recalled by...
The Issue: Zimmer Biomet is conducting a medical device field action for various...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Oxford Partial Knee System Right Medial Tibial Trial Tray Size Recalled by...
The Issue: Zimmer Biomet is conducting a medical device field action for various...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Oxford Partial Knee System Left Medial Tibial Trial Tray Size Recalled by...
The Issue: Zimmer Biomet is conducting a medical device field action for various...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Oxford Unicompartmental Knee Phase 3 Shim Size 3 Product Usage: Recalled by...
The Issue: Zimmer Biomet is conducting a medical device field action for various...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Oxford Unicompartmental Knee Phase 3 Shim Size 1 Product Usage: Recalled by...
The Issue: Zimmer Biomet is conducting a medical device field action for various...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Oxford Partial Knee System Left Medial Tibial Trial Tray Size Recalled by...
The Issue: Zimmer Biomet is conducting a medical device field action for various...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Oxford Unicompartmental Knee Phase 3 Shim Size 2 Product Usage: Recalled by...
The Issue: Zimmer Biomet is conducting a medical device field action for various...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Oxford Unicompartmental Knee Phase 3 Tibial Impactor Product Usage:...
The Issue: Zimmer Biomet is conducting a medical device field action for various...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Oxford Partial Knee System Phase 3 Tibial Template Right Medial Recalled by...
The Issue: Zimmer Biomet is conducting a medical device field action for various...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.