Product Recalls in California
Product recalls affecting California — including food, drugs, consumer products, medical devices, and vehicles distributed to California. RecallDetector monitors distribution data from the FDA, USDA, CPSC, and NHTSA to show you which recalls are relevant to your area. 1,048 recalls have been distributed to California in the last 12 months.
Showing 39461–39480 of 56,506 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: 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: 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: 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: 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: Bard Distaflo Vascular Bypass Graft Recalled by Bard Peripheral Vascular Inc...
The Issue: Size mislabeling; the graft is a 6 mm diameter graft when the actual...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Bard Distaflo Vascular Bypass Graft Recalled by Bard Peripheral Vascular Inc...
The Issue: Size mislabeling; the graft is labeled as a 6 mm diameter graft when the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Magnesium Sulfate in Water for Injection Recalled by Hospira Inc. Due to...
The Issue: Labeling: Incorrect Barcode: Primary bag labeling may be mislabeled with the...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Bromfenac Ophthalmic Solution 0.09% Recalled by Mayne Pharma Usa Due to Lack...
The Issue: Lack of Assurance of Sterility: Failed preservative effectiveness test
Recommended Action: Stop taking this medication. Contact your pharmacy or 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 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 Knee System Tibial Resector Body Tube & Guides Product 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.