Product Recalls in Texas

Product recalls affecting Texas — including food, drugs, consumer products, medical devices, and vehicles distributed to Texas. RecallDetector monitors distribution data from the FDA, USDA, CPSC, and NHTSA to show you which recalls are relevant to your area. 1,116 recalls have been distributed to Texas in the last 12 months.

55,713 total recalls
1,116 in last 12 months

Showing 16101–16120 of 30,921 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· Olympus Corporation of the Americas

Recalled Item: Bronchovideoscope BF-160 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· Zimmer Biomet, Inc.

Recalled Item: Affixus Hip Fracture Nail Left 125 11 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· 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 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.

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

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.

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 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· 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· Olympus Corporation of the Americas

Recalled Item: Bronchovideoscope BF-3C40 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· 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 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.

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

Recalled Item: Affixus Hip Fracture Nail Right 125 9 mm x 340 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· Implant Direct Sybron Manufacturing, LLC

Recalled Item: ImplantDirect Legacy 3 Implant Recalled by Implant Direct Sybron...

The Issue: Two units in distribution were found to be mislabeled on the vial cap with...

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 Left 125 9 mm x 300 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: Bronchofiberscope BF-P60 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· Zimmer Biomet, Inc.

Recalled Item: Affixus Hip Fracture Nail Left 130 15 mm x 360 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· Zimmer Biomet, Inc.

Recalled Item: Affixus Hip Fracture Nail Right 125 11 mm x 420 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 Left 125 11 mm x 320 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