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 41681–41700 of 50,591 recalls
Recalled Item: ASEPT 600 ml Drainage Kit Recalled by Pfm Medical Inc Due to PFM Medical is...
The Issue: PFM Medical is recalling catheters and other medical devices because they...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ASEPT 2000 ml Drainage Bag Recalled by Pfm Medical Inc Due to PFM Medical is...
The Issue: PFM Medical is recalling catheters and other medical devices because they...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: MAS CardioImmune XL Cardiac Marker Control Recalled by Microgenics...
The Issue: MAS CardioImmune XL, level 1 (lot CXL16011), is showing vial-to-vial...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ThermoCool SmartTouch Navigation Catheters Recalled by Biosense Webster,...
The Issue: The recall was initiated because Biosense Webster is providing additional...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Gabapentin Capsules Recalled by Aurobindo Pharma USA Inc Due to Failed...
The Issue: Failed Tablet/Capsule Specifications: Complaints of empty capsules received.
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Obagi Nu-Derm Clear Recalled by Obagi Medical Products Due to Labeling:...
The Issue: Labeling: Label Mix-Up; Containers of the Obagi Nu-Derm Clear pre-labeled...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Ethicon PERMA-HAND Silk siliconized black braided 10 strands per packet...
The Issue: Ethicon is unable to ensure that PERMA-HAND silk suture (siliconized black...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Rapid Neg Urine Combo Panel Type 1 Recalled by Siemens Healthcare...
The Issue: An increase in false positive susceptible results on Rapid Neg BP Combo...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Cardiohelp-I System Product Usage: A blood oxygenation and carbon dioxide...
The Issue: Cardiohelp- i System may have a software issue that can potentially result...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Rapid Neg BP Combo Panel Type 3 Recalled by Siemens Healthcare Diagnostics,...
The Issue: An increase in false positive susceptible results on Rapid Neg BP Combo...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: 1% LIDOCAINE HCl Injection Recalled by Hospira Inc. Due to Presence of...
The Issue: Presence of particulate matter: A returned customer sample was evaluated and...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Candesartan Cilexetil Tablets Recalled by Apotex Inc. Due to Failed...
The Issue: Failed Impurities/Degradation Specifications: Out of specification (OOS)...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Candesartan Cilexetil Tablets Recalled by Apotex Inc. Due to Failed...
The Issue: Failed Impurities/Degradation Specifications: Out of specification (OOS)...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Cyproheptadine HCl Syrup (Cyproheptadine HCl Oral Solution Recalled by...
The Issue: Failed Impurities/Degradation Specifications : Out-of-specification result...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Candesartan Cilexetil Tablets Recalled by Apotex Inc. Due to Failed...
The Issue: Failed Impurities/Degradation Specifications: Out of specification (OOS)...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Candesartan Cilexetil Tablets Recalled by Apotex Inc. Due to Failed...
The Issue: Failed Impurities/Degradation Specifications: Out of specification (OOS)...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Publix Asian Mix Recalled by Publix Bakery Plant Due to Product contains...
The Issue: Product contains peanuts that are not declared on the label.
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: MicroVue Bb Plus EIA is packaged as a kit which Recalled by Diagnostic...
The Issue: Samples are quantitating incorrectly, with approximately 50% higher...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Align Radial Stems Recalled by Skeletal Dynamics Due to Report received...
The Issue: Report received where the Align Radial Stem fractured.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Zimmer Patient Specific Instrument PERSONA CR Pin Guides (Femur and Recalled...
The Issue: The box of guides for a specific case arrived intact but contained two (2)...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.