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. 2,429 recalls have been distributed to Alabama in the last 12 months.
Showing 39141–39160 of 50,591 recalls
Recalled Item: Bio Armor CreaMatrix 60 servings Blue Raspberry Recalled by Reaction...
The Issue: Work out support nutritional supplements manufactured on shared equipment...
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Bio Armor CreaMatrix 60 servings Cherry Lime Recalled by Reaction Nutrition...
The Issue: Work out support nutritional supplements manufactured on shared equipment...
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: REACTION RECOR: Amino Action- 500g (Island Breeze) Recalled by Reaction...
The Issue: Work out support nutritional supplements manufactured on shared equipment...
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: RN BlueChip: Glutamine Recalled by Reaction Nutrition LLC Due to Work out...
The Issue: Work out support nutritional supplements manufactured on shared equipment...
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Flurandrenolide Tape Recalled by Actavis Laboratories Due to Subpotent Drug:...
The Issue: Subpotent Drug: Flurandrenolide is subpotent.
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Remote Network Station Recalled by Nihon Kohden America Inc Due to Nihon...
The Issue: Nihon Kohden America (NKA) is recalling the Remote Network Station (RNS)...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Philips Healthcare Ingenuity Core 128 Computed Tomography X-ray system...
The Issue: During scans with specific protocol steps, the software unexpectedly sets...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Philips Healthcare Ingenuity Core Computed Tomography X-ray system Recalled...
The Issue: During scans with specific protocol steps, the software unexpectedly sets...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: KimVent Turbo-Cleaning Closed Suction System for Adults Recalled by Halyard...
The Issue: The internal blue flapper valve of certain KimVent Turbo-Cleaning Closed...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Philips Healthcare Brilliance 64 Computed Tomography X-ray system Recalled...
The Issue: During scans with specific protocol steps, the software unexpectedly sets...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: AXIOM ARISTOS FX Recalled by Siemens Medical Solutions USA, Inc Due to If...
The Issue: If the cable cart and the corrugated hose are unable to move freely, the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Philips Healthcare Ingenuity CT Computed Tomography X-ray system Recalled by...
The Issue: During scans with specific protocol steps, the software unexpectedly sets...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: SIEMENS Luminos Agile Max Recalled by Siemens Medical Solutions USA, Inc Due...
The Issue: Study and all acquired images deleted when using systems with software...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: SIEMENS Axiom Luminos dRF Max Recalled by Siemens Medical Solutions USA, Inc...
The Issue: Study and all acquired images deleted when using systems with software...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: SIEMENS Uroskop Omnia Max Recalled by Siemens Medical Solutions USA, Inc Due...
The Issue: Study and all acquired images deleted when using systems with software...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: McKesson Medi-Pak Vaginal Speculum Recalled by CooperSurgical, Inc. Due to...
The Issue: Small sized specula were incorrectly packaged in printed bags for the medium...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: SIEMENS Ysio Max Recalled by Siemens Medical Solutions USA, Inc Due to Study...
The Issue: Study and all acquired images deleted when using systems with software...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Fluoxetine Capsules USP Recalled by Teva Pharmaceuticals USA Due to Chemical...
The Issue: Chemical Contamination: Product recalled due to an elevated level of a...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Ketorolac Tromethamine Inj. USP Recalled by Hospira Inc. Due to Crystallization
The Issue: Crystallization
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Ketorolac Tromethamine Inj. USP Recalled by Hospira Inc. Due to Crystallization
The Issue: Crystallization
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.