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. 2,660 recalls have been distributed to Texas in the last 12 months.
Showing 33341–33360 of 55,713 recalls
Recalled Item: LASEREDGE Knives Recalled by Bausch & Lomb Inc Irb Due to The complaints...
The Issue: The complaints database was reviewed and there have been an atypical volume...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: LASEREDGE Knives Recalled by Bausch & Lomb Inc Irb Due to The complaints...
The Issue: The complaints database was reviewed and there have been an atypical volume...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: LASEREDGE Knives Recalled by Bausch & Lomb Inc Irb Due to The complaints...
The Issue: The complaints database was reviewed and there have been an atypical volume...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: LASEREDGE Knives Recalled by Bausch & Lomb Inc Irb Due to The complaints...
The Issue: The complaints database was reviewed and there have been an atypical volume...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: LASEREDGE Knives Recalled by Bausch & Lomb Inc Irb Due to The complaints...
The Issue: The complaints database was reviewed and there have been an atypical volume...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: LASEREDGE Knives Recalled by Bausch & Lomb Inc Irb Due to The complaints...
The Issue: The complaints database was reviewed and there have been an atypical volume...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: LASEREDGE Knives Recalled by Bausch & Lomb Inc Irb Due to The complaints...
The Issue: The complaints database was reviewed and there have been an atypical volume...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: LASEREDGE Knives Recalled by Bausch & Lomb Inc Irb Due to The complaints...
The Issue: The complaints database was reviewed and there have been an atypical volume...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: LASEREDGE Knives Recalled by Bausch & Lomb Inc Irb Due to The complaints...
The Issue: The complaints database was reviewed and there have been an atypical volume...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ImplantDirect Recalled by Implant Direct Sybron Manufacturing, LLC Due to...
The Issue: The main vial label lists the incorrect part number, but the cap label is...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Vertebral Motion Analyzer (VMA) Recalled by Ortho Kinematics, Inc Due to...
The Issue: Ortho Kinematics notified customers that errors were contained in...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: eCare Coordinator Product Usage: is software intended for use in Recalled by...
The Issue: eCareCoordinator (eCC) is intended for use in data aggregation, patient...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Desonide Ointment Recalled by Fougera Pharmaceuticals Inc. Due to Labeling:...
The Issue: Labeling: Label Mixup; Unit boxes labeled as Desonide Ointment 0.05% may...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Double Hyaluronic 1000 Recalled by Signature Club A Ltd Due to Microbial...
The Issue: Microbial Contamination of Non-Sterile Products: odor complaint of product...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Cobas 8100 uni-directional (BRF) module with Software Version 02-xx Recalled...
The Issue: Roche Diagnostics Corp. initiated a voluntary correction because a rack...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Cobas 8100 bi-directional (BRF) module with Software Version 02-xx Recalled...
The Issue: "Roche Diagnostics Corp. initiated a voluntary correction because a rack...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Parmesan Truffle Salt. The product is packaged in glass taster Recalled by...
The Issue: Parmigiano Reggiano (Parmesan) cheese is declared, but milk is not listed on...
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Segmental vss bowed 19x190mm Recalled by Zimmer Biomet, Inc. Due to Zimmer...
The Issue: Zimmer Biomet Inc. initiated a field action on 02/28/2017 for...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Sterile Handpiece Sheaths Recalled by ConMed Corporation Due to For over a...
The Issue: For over a year, the Accessory Packages in the Hyfrecator 2000 ESU cartons...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Sterile Handpiece Sheaths Recalled by ConMed Corporation Due to For over a...
The Issue: For over a year, the Accessory Packages in the Hyfrecator 2000 ESU cartons...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.