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. 1,142 recalls have been distributed to Texas in the last 12 months.
Showing 13521–13540 of 30,921 recalls
Recalled Item: Quantam 2000 Electrosurgical Generator Recalled by CooperSurgical, Inc. Due...
The Issue: Potential for the Quantum 2000 Electrosurgery Generator, part numbers...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: BD Posiflush Pre-Filled Normal Saline Syringes Catalog Number: 306547...
The Issue: Limited number of syringes labeled Posiflush Experimental Product and Not...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: BD Posiflush Pre-Filled Normal Saline Syringes Catalog Number: 306575...
The Issue: Limited number of syringes labeled Posiflush Experimental Product and Not...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Urine Electrolyte Diluent Recalled by Ortho Clinical Diagnostics Inc Due to...
The Issue: Potential for the instability of the diluents VITROS 7% BSA (Product Code...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Radiofrequency Grounding Pad Recalled by Abbott Medical Due to Affected lots...
The Issue: Affected lots were manufactured with the protective release liner in an...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: 7% BSA (Bovine Serum Albumin) Recalled by Ortho Clinical Diagnostics Inc Due...
The Issue: Potential for the instability of the diluents VITROS 7% BSA (Product Code...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Levo Arm Label: LEVO ARM MIZUHO OSI Recalled by Mizuho OSI Due to Due to the...
The Issue: Due to the potential for fluid ingress into the Arm which could affect the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Implant Direct Recalled by Implant Direct Sybron Manufacturing LLC Due to...
The Issue: Through a customer complaint and and internal investigation it was...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Sprotte Needle Recalled by TELEFLEX MEDICAL INC Due to Teleflex received the...
The Issue: Teleflex received the attached Medical Device Recall Notice from Pajunk...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Berchtold Chromophare Ceiling Mounted Surgical Light System Recalled by...
The Issue: The firm has become aware that there is a likelihood that a missing snap...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Sprotte Needle Recalled by TELEFLEX MEDICAL INC Due to Teleflex received the...
The Issue: Teleflex received the attached Medical Device Recall Notice from Pajunk...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: The PolarCath Balloon Catheter consists of a coaxial catheter shaft Recalled...
The Issue: Peripheral Dilation Catheters that were E-Beam Sterilized were inadvertently...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: MEDICOM SAFEMASK PREMIER PLUS ASTM LEVEL 3 MASKS Recalled by AMD Medicom...
The Issue: Due to an error on the packaging line, some level 2 masks may have been...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ElectroTek Temporal Sensor Cable Gold - Long Length Recalled by LIFELINES...
The Issue: Potential for one of the four temporal electrode cables used in with the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ElectroTek Temporal Sensor Cable Gold - Long Length Recalled by LIFELINES...
The Issue: Potential for one of the four temporal electrode cables used in with the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: MEDICOM SAFEMASK PREMIER PLUS ASTM LEVEL 2 MASKS Recalled by AMD Medicom...
The Issue: Due to an error on the packaging line, some level 2 masks may have been...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: cable button for NCB¿ Polyaxial Locking Plate Recalled by Zimmer Biomet,...
The Issue: Non-highly polished implants may adhere to the LDPE bag (previous packaging...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Various Custom Devices Recalled by Zimmer Biomet, Inc. Due to Non-highly...
The Issue: Non-highly polished implants may adhere to the LDPE bag (previous packaging...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Sidus Stem-Free Shoulder Humeral Head Recalled by Zimmer Biomet, Inc. Due to...
The Issue: Non-highly polished implants may adhere to the LDPE bag (previous packaging...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Cephalomedullary Nail (CMN) Recalled by Zimmer Biomet, Inc. Due to...
The Issue: Non-highly polished implants may adhere to the LDPE bag (previous packaging...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.