Product Recalls in Oklahoma
Product recalls affecting Oklahoma — including food, drugs, consumer products, medical devices, and vehicles distributed to Oklahoma. RecallDetector monitors distribution data from the FDA, USDA, CPSC, and NHTSA to show you which recalls are relevant to your area. 2,496 recalls have been distributed to Oklahoma in the last 12 months.
Showing 21101–21120 of 28,654 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: Single Lumen Central Venous Catheter Sets and Trays The subject Recalled by...
The Issue: A manufacturing process may lead to catheter tip fracture and or separation....
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 Phase 3 Tibial Template Left 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.
Recalled Item: InVision-Plus CS Needleless IV Connector Recalled by Rymed Technologies, LLC...
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 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 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 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 Femoral Slap Hammer Product Usage: Instruments...
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 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.
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 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.
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.