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. 2,064 recalls have been distributed to Alabama in the last 12 months.
Showing 6981–7000 of 50,591 recalls
Recalled Item: Acu-Loc and Acu-Loc 2 bone plates Recalled by Acumed LLC Due to Distribution...
The Issue: Distribution without Pre-Market Clearance
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Ministry of Snacks Sweet and Savory Collection #8700 Recalled by Houdini...
The Issue: Potential Salmonella contamination of Quaker Oats Chewy Granola Bars packed...
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Shiloh Farms Organic Salt Free 7 Grain Bread Recalled by Garden Spot Foods,...
The Issue: Daily recommended consumption of Cholesterol and Sodium are listed in grams...
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Shiloh Farms Bread for Life Organic 7 Grain Recalled by Garden Spot Foods,...
The Issue: Daily recommended consumption of Cholesterol and Sodium are listed in grams...
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Shiloh Farms Organic 7 Grain Bread Recalled by Garden Spot Foods, LLC. Due...
The Issue: Daily recommended consumption of Cholesterol and Sodium are listed in grams...
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: TactiFlex Ablation Sensor Enabled Ablation Catheter Recalled by St. Jude...
The Issue: When the catheters are used with the EnSiteX EP System, the system does not...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Vortex Surgical ACTU8 FORCEPS Recalled by Vortex Surgical Inc. Due to Reason...
The Issue: Reason for the voluntary recall is residue was identified on the two forceps...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ExcelsiusGPS Cannula A Recalled by Globus Medical, Inc. Due to Devices may...
The Issue: Devices may not be rendered sterile due to an internal gap that may be...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: BrightView XCT Recalled by Philips North America Due to Detector may...
The Issue: Detector may unexpectedly fall due to a component failure. If the detector...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: PANTHER FUSION System The Panther System is an Recalled by Hologic, Inc. Due...
The Issue: Due to potential false positive Flu B results when a sample was also...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Total immunoglobulin M (IgM total) IVD Recalled by Siemens Healthcare...
The Issue: Potential for a negative bias with quality control (QC) and patient sample...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: BrightView X Recalled by Philips North America Due to Detector may...
The Issue: Detector may unexpectedly fall due to a component failure. If the detector...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ProxiDiagnost upgrade- A Multi-functional general Radiography and...
The Issue: Issue 1: Mixed Images: The Radio Fluoroscopy (RF) viewer may also display a...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ProxiDiagnost N90- A Multi-functional general Radiography and Fluoroscopy...
The Issue: Issue 1: Mixed Images: The Radio Fluoroscopy (RF) viewer may also display a...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: BrightView Recalled by Philips North America Due to Detector may...
The Issue: Detector may unexpectedly fall due to a component failure. If the detector...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ESG PK CUTTING FORCEPS Recalled by Olympus Corporation of the Americas Due...
The Issue: The jaw may fracture prior to the procedure during the inspection instructed...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Publix Custom Burrito Bowls Recalled by Publix Super Markets, Inc. Due to...
The Issue: The underlying ingredient, shredded lettuce, was recalled by the supplier...
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Tacrolimus Capsules Recalled by Dr. Reddy's Laboratories, Inc. Due to...
The Issue: Presence of Foreign Tablets/Capsules: One 0.5 mg Tacrolimus capsule found in...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Publix Custom Made Sub Sandwiches Recalled by Publix Super Markets, Inc. Due...
The Issue: The underlying ingredient, shredded lettuce, was recalled by the supplier...
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Publix Deli Chicken Street Tacos for Two Recalled by Publix Super Markets,...
The Issue: The underlying ingredient, shredded lettuce, was recalled by the supplier...
Recommended Action: Do not consume. Return to store for a refund or discard.