Product Recalls in Alabama
Product recalls affecting Alabama — including food, drugs, consumer products, medical devices, and vehicles distributed to Alabama. RecallDetector monitors distribution data from the FDA, USDA, CPSC, and NHTSA to show you which recalls are relevant to your area. 2,467 recalls have been distributed to Alabama in the last 12 months.
Showing 31421–31440 of 50,591 recalls
Recalled Item: Pharmanex ageLOC TR90 Protein Boost. Protein Powder. Net wt. 1.59 Recalled...
The Issue: Nu Skin announces a voluntary field action for Pharmanex ageLOC TR90 Protein...
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Valleylab Laparoscopic Handset Recalled by COVIDIEN MEDTRONIC Due to...
The Issue: Customer reports of the device handset continuing to operate after release...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: The ABL800 Model#:All Recalled by Radiometer America Inc Due to Reports that...
The Issue: Reports that the sample type "cord blood" has been changed into the two...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ABL90 Flex Model #: 393-090 Portable Recalled by Radiometer America Inc Due...
The Issue: Reports that the sample type "cord blood" has been changed into the two...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: MEVATRON MD-2 Recalled by Siemens Medical Solutions USA, Inc Due to Siemens...
The Issue: Siemens became aware of a defective weld seam at overhead suspensions. Due...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: PRIMUS HI and Mevatron M2/Primus Mid-Energy Recalled by Siemens Medical...
The Issue: Siemens became aware of a defective weld seam at overhead suspensions. Due...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Influenza Transport Swab Packages Recalled by Quidel Corporation Due to...
The Issue: Quidel Corporation is recalling Influenza Transport Swab Packages because it...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: MEVATRON M 6730/6740 (MEX) Accelerator Recalled by Siemens Medical Solutions...
The Issue: Siemens became aware of a defective weld seam at overhead suspensions. Due...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: MEVATRON M 7400/7440(MEX) Accelerator Recalled by Siemens Medical Solutions...
The Issue: Siemens became aware of a defective weld seam at overhead suspensions. Due...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: MEVATRON M 6700 (MX) Accelerator Recalled by Siemens Medical Solutions USA,...
The Issue: Siemens became aware of a defective weld seam at overhead suspensions. Due...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: MEVATRON KD-2 Recalled by Siemens Medical Solutions USA, Inc Due to Siemens...
The Issue: Siemens became aware of a defective weld seam at overhead suspensions. Due...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: The UNI-CP System Recalled by Integra LifeSciences Corp. Due to The firm...
The Issue: The firm received one complaint from one non-US sales representative...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Vancomycin Hydrochloride for Injection Recalled by Hospira Inc., A Pfizer...
The Issue: Presence of Particulate Matter: A hair was found stuck to the stopper of...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: XTRAC Excimer Laser Recalled by Strata Skin Sciences, Inc. Due to When the...
The Issue: When the Liquid Guide ( LLG) is not used according to the operator manual,...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Premier Guard Drape Recalled by Covidien LLC Due to Sterility compromised...
The Issue: Sterility compromised due to breach in sterile barrier
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Premier Guard Sterile Drape For Use with Blair-Port Wand (02-0029) Recalled...
The Issue: Sterility compromised due to breach in sterile barrier
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Blastomyces dermatitidis Antiserum 1 mL vial GIBSON BIOSCIENCE. Catalog...
The Issue: The firm information that the product was reporting false positive results
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Integra Cadence Total Ankle System Recalled by Integra LifeSciences Corp....
The Issue: Posterior tibial fractures have been reported.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Atrium PVC 10 Fr Straight Thoracic Catheter Code Number: 8010 Recalled by...
The Issue: Labeling icon depicts a catheter having six (6) eyelets; however the correct...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: CaviWipes1 Extra Large Recalled by Metrex Research, LLC. Due to Metrex is...
The Issue: Metrex is recalling the CaviWipes Extra Large because they may have been...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.