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. 2,585 recalls have been distributed to Texas in the last 12 months.
Showing 49001–49020 of 55,713 recalls
Recalled Item: GE Optima XR220amx and Optima XR200amx with Digital Upgrade Mobile Recalled...
The Issue: There exists a software issue associated with patient selection from the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: EOS System X- ray beam Digital radiography system used in Recalled by EOS...
The Issue: EOS imaging discovered during production internal testing that the X-ray...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: OrthoPediatrics ACL Reconstruction System is a pediatric and small stature...
The Issue: Part # 01-1008-0040/0047, ACL Sleeve Installation/ Insertion Tool, shipped...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Clonazepam Tablets Recalled by Actavis Elizabeth LLC Due to Subpotent Drug:...
The Issue: Subpotent Drug: During routine stability testing one tablet was found with...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Sumatriptan Succinate Injection Recalled by GlaxoSmithKline, LLC. Due to...
The Issue: Lack of Assurance of Sterility: A small number of pre-filled syringes may...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Imitrex STATdose System Recalled by GlaxoSmithKline, LLC. Due to Lack of...
The Issue: Lack of Assurance of Sterility: A small number of pre-filled syringes may...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Bumetanide Tablets USP 0.5 mg. Rx Only Recalled by Sandoz Inc Due to Failed...
The Issue: Failed Moisture Limit; Out of Specification (OOS) results were obtained for...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Siemens ADVIA Chemistry Systems models 1200 Recalled by Siemens Healthcare...
The Issue: The ADVIA Chemistry software systems using certain software versions allows...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: IMMULITE/IMMULITE 1000 Systems FOL Folic Acid Recalled by Siemens Healthcare...
The Issue: potential for an accelerated decline in counts per second (CPS) for three...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Instrument Manager driver : Driver sysu100i that connects to the Recalled by...
The Issue: When connected to the Sysmex UF-100, the Instrument Manager driver sysu100i...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Axillent Debakey Grasping Forceps Recalled by Karl Storz Endoscopy America...
The Issue: KARL STORZ is recalling the Axillent Debakey Grasping Forceps because the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Candela Laser GentleLase Pro Recalled by Candela Corporation Due to...
The Issue: Unintended single pulse maybe emitted to handpiece prior to pressing of...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: sertraline HCl tablets Recalled by Greenstone LLC Due to Labeling: Incorrect...
The Issue: Labeling: Incorrect or Missing Lot No. and/or Exp Date: Expiration date...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: SEAC Advanced Dental System Recalled by ASI Medical, Inc. Due to ASI Medical...
The Issue: ASI Medical is initiating a field correction for the SEAC Advanced Dental...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Navigator HD l3F/15F x 46cm Ureteral Access Sheath Set Product No...
The Issue: The 13F/15F Navigator HD Ureteral Access SheathSet are being recalled after...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Navigator HD l3F/15F x 36cm Ureteral Access Sheath Set Product No...
The Issue: The 13F/15F Navigator HD Ureteral Access SheathSet are being recalled after...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Navigator HD l3F/15F x 28 cm Ureteral Access Sheath Set Product No...
The Issue: The 13F/15F Navigator HD Ureteral Access SheathSet are being recalled after...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Glipizide XL (glipizide) extended release tablets Recalled by Greenstone Llc...
The Issue: Failed Dissolution Specification; the bulk lot yielded an out of...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Glucotrol XL (glipizide) extended release tablets Recalled by Pfizer Inc....
The Issue: Failed Dissolution Specification; 8 hr stability timepoint
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Soliris (eculizumab) Concentrated Solution for Intravenous Infusion Only...
The Issue: Presence of Particulate Matter: Failed the appearance test for the presence...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.