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. 1,042 recalls have been distributed to Texas in the last 12 months.
Showing 36301–36320 of 55,713 recalls
Recalled Item: Bulk flour bland breader packaged into 15 Recalled by Newly Weds Foods Inc...
The Issue: Flour contaminated with E. coli O121 was used in the manufacuring of flour...
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: FE RedBell Pepper Recalled by QualiTech, Inc Due to Potential E. coli...
The Issue: QualiTech has been notified by a supplier that they received material with...
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: FE Green Bell Pepper Recalled by QualiTech, Inc Due to Potential E. coli...
The Issue: QualiTech has been notified by a supplier that they received material with...
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: FE Bacon 286 Recalled by QualiTech, Inc Due to Potential E. coli Contamination
The Issue: QualiTech has been notified by a supplier that they received material with...
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: FE Cheddar Cheese Recalled by QualiTech, Inc Due to Potential E. coli...
The Issue: QualiTech has been notified by a supplier that they received material with...
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: RePlant¿ Angled Abutment Part Number 6050-52-60 Recalled by Implant Direct...
The Issue: Issue with design specification; oversized condition.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Siemens RAPIDPoint¿ 500 v2.2.2A Software Upgrade Kit Recalled by Siemens...
The Issue: Some v2.2.2 upgrade kits include a dialysate mode which not cleared/approved...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: AmediCheck Instant Test Cup Recalled by Branan Medical Corporation Due to...
The Issue: Branan Medical is recalling the AmediCheck Instant Test Cup, a 5 panel drug...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Oxygen Nasal Wash (purified water Recalled by Let's Talk Health, Inc. Due to...
The Issue: Marketed Without An Approved NDA/ANDA: product is an unapproved drug due to...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Zimmer¿ Air Dermatome II Width Plate Recalled by Zimmer Surgical Inc Due to...
The Issue: The surface coating applied to the device is blistering, peeling and...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Zimmer¿ Air Dermatome II Width Plate Recalled by Zimmer Surgical Inc Due to...
The Issue: The surface coating applied to the device is blistering, peeling and...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Zimmer¿ Air Dermatome II Handpiece Loaner Recalled by Zimmer Surgical Inc...
The Issue: Zimmer Biomet Surgical has received product complaints reporting that the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Zimmer¿ Air Dermatome II Width Plate Recalled by Zimmer Surgical Inc Due to...
The Issue: The surface coating applied to the device is blistering, peeling and...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Zimmer¿ Air Dermatome II Handpiece Recalled by Zimmer Surgical Inc Due to...
The Issue: The surface coating applied to the device is blistering, peeling and...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Zimmer¿ Air Dermatome II Width Plate Recalled by Zimmer Surgical Inc Due to...
The Issue: The surface coating applied to the device is blistering, peeling and...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Zimmer¿ Air Dermatome II Handpiece w/o Hose Recalled by Zimmer Surgical Inc...
The Issue: The surface coating applied to the device is blistering, peeling and...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Zimmer¿ Air Dermatome II Width Plate Recalled by Zimmer Surgical Inc Due to...
The Issue: The surface coating applied to the device is blistering, peeling and...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Fluorocell PLT reagent Recalled by Sysmex America Inc Due to There is a...
The Issue: There is a potential that fluorescent platelet (PLT-F) and immature platelet...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: The Better-Bladder With 14" ID tubing Recalled by Circulatory Technology Inc...
The Issue: Twisted or wrinkled balloon components which are considered a cosmetic...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Mentor MemoryGel Breast Implant Recalled by Mentor Texas, LP. Due to The box...
The Issue: The box of 300cc MemoryGel Breast Implant was labeled with null...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.