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. 2,697 recalls have been distributed to Texas in the last 12 months.
Showing 20501–20520 of 30,921 recalls
Recalled Item: Bio-Stable 5F DL-55CM IR-145 Kit Valved PG Recalled by Angiodynamics Inc....
The Issue: Navilyst Medical, Inc. (NMI) the manufacturer of the Xcela PICC with PASV,...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Bio-Stable 5F DL-55CM MST-70 KIT Non-Valved w/ Nit GW Recalled by...
The Issue: Navilyst Medical, Inc. (NMI) the manufacturer of the Xcela PICC with PASV,...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Xcela PICC Kit with ENDEXO and PASV Valve Technology Recalled by...
The Issue: Navilyst Medical, Inc. (NMI) the manufacturer of the Xcela PICC with PASV,...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Bio-Stable 5F SL-55CM IR-145 Kit Valved PG Recalled by Angiodynamics Inc....
The Issue: Navilyst Medical, Inc. (NMI) the manufacturer of the Xcela PICC with PASV,...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: MagSIL (NucliSENS easyMAG Magnetic Silica) Recalled by BioMerieux SA Due to...
The Issue: A drift of the performance with the BK test (BK virus, worst case...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: NucliSENS magnetic extraction reagents Recalled by BioMerieux SA Due to A...
The Issue: A drift of the performance with the BK test (BK virus, worst case...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Straumann Twist Drill PRO ¿4.2mm Recalled by Straumann Manufacturing, Inc....
The Issue: Drills cannot be inserted into handpiece due to tolerance specification not met
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Straumann Drill 1 Recalled by Straumann Manufacturing, Inc. Due to Drills...
The Issue: Drills cannot be inserted into handpiece due to tolerance specification not met
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Unna-Z Recalled by Medline Industries Inc Due to Medline Industries, Inc is...
The Issue: Medline Industries, Inc is recalling Unna Z Unna Boot Bandage 3 X10 and...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Optimus Fixed Awl Recalled by Amendia, Inc Due to Complaints that the tip of...
The Issue: Complaints that the tip of the awl broke after impaction during surgery.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Black Widow Plate 19mm Plate Recalled by Amendia, Inc Due to There is a...
The Issue: There is a problem with the mating feature between the plate and screw which...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Black Widow 6.6mm x 20mm Screw Recalled by Amendia, Inc Due to There is a...
The Issue: There is a problem with the mating feature between the plate and screw which...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: RUSCH Recalled by Teleflex Medical Due to Labeling Inconsistency: The...
The Issue: Labeling Inconsistency: The products have been labeled with the incorrect...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: SIEMENS IMMULITE 2000/2000 Xpi Systems Intact PTH (Parathyroid Hormone) Test...
The Issue: Siemens is conducting this recall for the IMMULITE¿ 2000/IMMULITE¿ 2000 XPi...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: K-Wire 1.4mm x 12in Non-Threaded Recalled by Amendia, Inc Due to The rods...
The Issue: The rods are packaged in packages with unacceptable seals. In some cases,...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Halo Closed System Transfer Device Recalled by J&J Solutions, Inc. DBA...
The Issue: Product malfunction: Needle does not retract.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Savannah-T Straight Rod Recalled by Amendia, Inc Due to The rods are...
The Issue: The rods are packaged in packages with unacceptable seals. In some cases,...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: G3 Opticage Expandable Interbody Fusion Device Recalled by Interventional...
The Issue: During implantation, the proximal end of the device could separate if the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Dual Stylet Needle Recalled by Amendia, Inc Due to The rods are packaged in...
The Issue: The rods are packaged in packages with unacceptable seals. In some cases,...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Zeus-P Lumbar Interbody Device Recalled by Amendia, Inc Due to Labeling...
The Issue: Labeling error where three boxes in inventory had conflicting patient and...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.