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. 2,839 recalls have been distributed to California in the last 12 months.

56,506 total recalls
2,839 in last 12 months

Showing 2700127020 of 56,506 recalls

Medical DeviceAugust 8, 2018· Bausch & Lomb Inc

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.

Class II — Potential Health HazardOngoing
Medical DeviceAugust 8, 2018· Bausch & Lomb Inc

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.

Class II — Potential Health HazardOngoing
Medical DeviceAugust 8, 2018· Bausch & Lomb Inc

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.

Class II — Potential Health HazardOngoing
Medical DeviceAugust 8, 2018· Bausch & Lomb Inc

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.

Class II — Potential Health HazardOngoing
Medical DeviceAugust 8, 2018· Zimmer Biomet, Inc.

Recalled Item: Affixus Hip Fracture Nail Right 125 9 mm x 460 mm Recalled by Zimmer Biomet,...

The Issue: There were complaints indicating that when the product was opened in...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceAugust 8, 2018· Olympus Corporation of the Americas

Recalled Item: Bronchofibercope BF-6C240 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.

Class II — Potential Health HazardOngoing
Medical DeviceAugust 8, 2018· Zimmer Biomet, Inc.

Recalled Item: Affixus Hip Fracture Nail 130 11 mm x 180 mm Recalled by Zimmer Biomet, Inc....

The Issue: There were complaints indicating that when the product was opened in...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceAugust 8, 2018· Zimmer Biomet, Inc.

Recalled Item: Affixus Hip Fracture Nail Right 130 13 mm x 360 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.

Class II — Potential Health HazardOngoing
Medical DeviceAugust 8, 2018· Bausch & Lomb Inc

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.

Class II — Potential Health HazardOngoing
Medical DeviceAugust 8, 2018· Zimmer Biomet, Inc.

Recalled Item: Affixus Hip Fracture Nail Right 130 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.

Class II — Potential Health HazardOngoing
Medical DeviceAugust 8, 2018· Zimmer Biomet, Inc.

Recalled Item: Affixus Hip Fracture Nail Right 125 13 mm x 400 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.

Class II — Potential Health HazardOngoing
Medical DeviceAugust 8, 2018· Olympus Corporation of the Americas

Recalled Item: Bronchovideoscope BF-Q180 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.

Class II — Potential Health HazardOngoing
Medical DeviceAugust 8, 2018· Zimmer Biomet, Inc.

Recalled Item: Affixus Hip Fracture Nail Left 125 13 mm x 260 mm Recalled by Zimmer Biomet,...

The Issue: There were complaints indicating that when the product was opened in...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceAugust 8, 2018· Olympus Corporation of the Americas

Recalled Item: Bronchovideoscope BF-240 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.

Class II — Potential Health HazardOngoing
Medical DeviceAugust 8, 2018· Olympus Corporation of the Americas

Recalled Item: Rhino Laryngo scope ENF-VT2 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.

Class II — Potential Health HazardOngoing
Medical DeviceAugust 8, 2018· Olympus Corporation of the Americas

Recalled Item: Bronchovideoscope BF-XP160F 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.

Class II — Potential Health HazardOngoing
Medical DeviceAugust 8, 2018· Zimmer Biomet, Inc.

Recalled Item: Affixus Hip Fracture Nail Left 125 9 mm x 460 mm Recalled by Zimmer Biomet,...

The Issue: There were complaints indicating that when the product was opened in...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceAugust 8, 2018· Olympus Corporation of the Americas

Recalled Item: Bronchovideoscope BF-3C160 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.

Class II — Potential Health HazardOngoing
Medical DeviceAugust 8, 2018· Olympus Corporation of the Americas

Recalled Item: Bronchovideoscope BF-MP160F 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.

Class II — Potential Health HazardOngoing
Medical DeviceAugust 8, 2018· Zimmer Biomet, Inc.

Recalled Item: Affixus Hip Fracture Nail Right 125 9 mm x 260 mm Recalled by Zimmer Biomet,...

The Issue: There were complaints indicating that when the product was opened in...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing