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. 1,152 recalls have been distributed to California in the last 12 months.
Showing 16201–16220 of 30,923 recalls
Recalled Item: Affixus Hip Fracture Nail Right 125 11 mm x 340 mm Recalled by Zimmer...
The Issue: There were complaints indicating that when the product was opened in...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Bausch + Lomb Stellaris Elite 23 GA Vit Cutter Recalled by Bausch & Lomb Inc...
The Issue: The back cap separates from the body of the vitrectomy cutter.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Bausch + Lomb Stellaris Elite 20 GA Vit Cutter Recalled by Bausch & Lomb Inc...
The Issue: The back cap separates from the body of the vitrectomy cutter.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Bausch + Lomb Stellaris Elite Vision Enhancement System Recalled by Bausch &...
The Issue: The back cap separates from the body of the vitrectomy cutter.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Bausch + Lomb Stellaris Elite Vision Enhancement System Recalled by Bausch &...
The Issue: The back cap separates from the body of the vitrectomy cutter.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Philips HeartStart Infant/Child SMART Pads Cartridge Recalled by Philips...
The Issue: The recall is being initiated due to incorrect age range labeling (8+ yrs)...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Bausch + Lomb Stellaris Elite Vision Enhancement System Recalled by Bausch &...
The Issue: The back cap separates from the body of the vitrectomy cutter.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Bausch + Lomb Stellaris Elite 25 GA Vit Cutter Recalled by Bausch & Lomb Inc...
The Issue: The back cap separates from the body of the vitrectomy cutter.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Magellan LeadCare¿ II Blood Lead Test Kit. In Vitro Test Recalled by...
The Issue: Defect with the calibration button for lot 1808M. Level 1 and Level 2...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Bausch + Lomb Stellaris Elite Vision Enhancement System Recalled by Bausch &...
The Issue: The back cap separates from the body of the vitrectomy cutter.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Bausch + Lomb Stellaris Elite Vision Enhancement System Recalled by Bausch &...
The Issue: The back cap separates from the body of the vitrectomy cutter.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Bausch + Lomb Stellaris Elite Vision Enhancement System Recalled by Bausch &...
The Issue: The back cap separates from the body of the vitrectomy cutter.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Bronchofiberscope BF-40 Recalled by Olympus Corporation of the Americas Due...
The Issue: The attachment of non-Olympus accessories to the bronchoscope s instrument...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Bronchovideoscope BF-1T180 Recalled by Olympus Corporation of the Americas...
The Issue: The attachment of non-Olympus accessories to the bronchoscope s instrument...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Bronchovideoscope BF-MP60 Recalled by Olympus Corporation of the Americas...
The Issue: The attachment of non-Olympus accessories to the bronchoscope s instrument...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Ultrasonic Bronchoscope BF-UC180F Recalled by Olympus Corporation of the...
The Issue: The attachment of non-Olympus accessories to the bronchoscope s instrument...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Bronchofiberscope BF-P40 Recalled by Olympus Corporation of the Americas Due...
The Issue: The attachment of non-Olympus accessories to the bronchoscope s instrument...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Bronchovideoscope BF-P180 Recalled by Olympus Corporation of the Americas...
The Issue: The attachment of non-Olympus accessories to the bronchoscope s instrument...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Extra corporeal circuit with bio-active surface. Recalled by Medtronic...
The Issue: Affected products failed a sterilization test.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Minimed Model 503 Remote Transmitter (MMT-503 Recalled by Medtronic Inc. Due...
The Issue: There is a potential security vulnerability related to the use of the remote...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.