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. 2,636 recalls have been distributed to Alabama in the last 12 months.
Showing 10761–10780 of 50,591 recalls
Recalled Item: API STAPH 25 STRIPS+25 MEDIA Recalled by Biomerieux Inc Due to As the...
The Issue: As the temperature and time out of range was exceeded, product performances...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ARTISTE Recalled by Siemens Medical Solutions USA, Inc Due to When selecting...
The Issue: When selecting the site fraction group for treatment, the User may select...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: FoundationOne CDx (F1CDx) Recalled by Foundation Medicine, Inc. Due to...
The Issue: Reports were sent to customers without the companion diagnostic (CDx) Claims...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: FoundationOne Liquid CDx (F1LCDx) Recalled by Foundation Medicine, Inc. Due...
The Issue: Reports were sent to customers without the companion diagnostic (CDx) Claims...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: 9 Gauge Disposable Trocars with Blunt Pushers for Use with Recalled by ENDO...
The Issue: No expiration dates printed on the packaging
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Corin BIOLOX DELTA MOD HEAD Recalled by Corin Ltd Due to The BIOLOX Delta...
The Issue: The BIOLOX Delta Ceramic Head size 36XL is labelled as the size 32XL and...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Corin BIOLOX DELTA MOD HEAD Recalled by Corin Ltd Due to The BIOLOX Delta...
The Issue: The BIOLOX Delta Ceramic Head size 36XL is labelled as the size 32XL and...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: InPen Diabetes Management App Recalled by Companion Medical, Inc. Due to...
The Issue: Diabetes management app may crash immediately upon opening, while using the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Betty Buzz Sparkling Grapefruit - Non-alcoholic Beverage & Mixer Container...
The Issue: Beverage has off-odor
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: R&D CBC-3D Hematology Control: (1) CBC-3D Normal Pack Hematology Control...
The Issue: For one lot of CBC-3D Hematology Control, the Normal Level may exhibit...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Cordis Angiographic Catheter Extensions. Used to transport fluid from the...
The Issue: There is a potential for separation at the male connector.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Flow-c Anesthesia System (Product Code 6887700) Flow-e Anesthesia System...
The Issue: The power backup battery, under certain conditions, may exhibit reduced...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Adam's Polishes ALCOHOL BASED HAND SANITIZER Recalled by Adam's Polishes LLC...
The Issue: CGMP Deviations: Other lots of hand sanitizer are being recalled because...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Adam's Polishes ALCOHOL BASED HAND SANITIZER Recalled by Adam's Polishes LLC...
The Issue: Chemical Contamination: FDA analysis found 1 lot of Adam's Polishes ALCOHOL...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Medical Action INDUSTRIES INC. Port a Cath Kit Recalled by Medical Action...
The Issue: XXX
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: IMMULITE 2000 Systems 3gAllergy Specific IgE Universal Kit Tests Japan...
The Issue: Potential for falsely elevated specific IgE mold allergen reactivity with...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: IMMULITE 2000 Systems 3gAllergy Specific IgE Universal Kit Tests (600T)-...
The Issue: Potential for falsely elevated specific IgE mold allergen reactivity with...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: IMMULITE 2000 Systems 3gAllergy Specific IgE Universal Kit Tests OUS...
The Issue: Potential for falsely elevated specific IgE mold allergen reactivity with...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: HF Resection Electrodes Recalled by Olympus Corporation of the Americas Due...
The Issue: An incompatible HF cable may be packaged with the HF Resection Electrodes....
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Nestle Toll House Edible Chocolate Chip Cookie Dough packaged in Recalled by...
The Issue: Potential of foreign material within product.
Recommended Action: Do not consume. Return to store for a refund or discard.