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 28361–28380 of 50,591 recalls
Recalled Item: Ninjacof-A (Acetaminophen 160 mg Recalled by Centurion Labs, LLC Due to...
The Issue: Microbial contamination of Non-sterile Products; potential B. cepacia...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Medfusion Recalled by Smiths Medical ASD Inc. Due to Potential for the...
The Issue: Potential for the syringe barrel clamp mechanism to loosen, decreasing the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Ziptight Ankle Syndesmosis Fixation Device Recalled by Zimmer Biomet, Inc....
The Issue: Ziptight Ankle Syndesmosis Fixation was packaged without the tip protectors.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Medfusion Recalled by Smiths Medical ASD Inc. Due to Potential for the...
The Issue: Potential for the syringe barrel clamp mechanism to loosen, decreasing the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Artis oneFloor-mounted system for uncompromised imaging Recalled by Siemens...
The Issue: The possibility exists for the monitor display of Artis one systems with a...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: AQUIOS CL Flow Cytometer System The AQUIOS CL Flow Cytometer Recalled by...
The Issue: Beckman Coulter has identified that an incorrect setting using a proprietary...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Azurion 3 M12 Recalled by Philips Electronics North America Corporation Due...
The Issue: When using the downscale option with the Allura R9 system or Azurion R1.1...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Xper Flex Cardio Physiomonitoring system. Used to facilitate invasive...
The Issue: Intermittent communication between the host system and the FlexCardio
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Syngo.plaza Picture Archiving and Communication System (PACS) with software...
The Issue: Software update to correct several issues that include (1)Potential data...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: TCC-EZ Recalled by Integra LifeSciences Corp. Due to A quarantined lot of...
The Issue: A quarantined lot of the devices was released for sale. Devices from this...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: A20975A "Working insert Recalled by Olympus Corporation of the Americas Due...
The Issue: Olympus has received complaints about fragments of adhesive which detached...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Paroxetine tablets USP Recalled by Zydus Pharmaceuticals USA Inc Due to...
The Issue: Presence of Foreign tablets/capsules: risperidone Tablets were found in...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Hydrocodone Bitartrate and Acetaminophen Oral Solution 7.5 mg/325 mg per...
The Issue: Labeling: Not Elsewhere Classified; product is incorrectly labeled as Class...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: All Sterile Products within expiry Recalled by Vital Rx, Inc. dba Atlantic...
The Issue: Lack of Assurance of Sterility .
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Java Monster Loco Moca Coffee & Energy Recalled by Monster Energy Company...
The Issue: Product was distributed without going through the retort step.
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Rajbhog Sweet Recalled by Rajbhog Distributors GA Inc Due to Undeclared Allergen
The Issue: Undeclared Allergen, Almond.
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Phenylephrine2.5%/Tropicamide 1% Ophthalmic Solution Recalled by Bella...
The Issue: Lack of Assurance of Sterility.
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Magnesium Chloride 200mg Recalled by Bella Pharmaceuticals, Inc. Due to Lack...
The Issue: Lack of Assurance of Sterility.
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: G.A.C 25/100/250mg Recalled by Bella Pharmaceuticals, Inc. Due to Lack of...
The Issue: Lack of Assurance of Sterility.
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Calcium chloride 10% Recalled by Bella Pharmaceuticals, Inc. Due to Lack of...
The Issue: Lack of Assurance of Sterility.
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.