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. 2,483 recalls have been distributed to Alabama in the last 12 months.

50,591 total recalls
2,483 in last 12 months

Showing 2448124500 of 50,591 recalls

DrugSeptember 7, 2018· Noven Pharmaceuticals, Inc.

Recalled Item: Minivelle (estradiol transdermal system) Patches Recalled by Noven...

The Issue: Defective Delivery System: out of specification results for shear, an...

Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.

Class II — Potential Health HazardOngoing
Refund
DrugSeptember 7, 2018· Noven Pharmaceuticals, Inc.

Recalled Item: Minivelle (estradiol transdermal system) Patches Recalled by Noven...

The Issue: Defective Delivery System: out of specification results for shear, an...

Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.

Class II — Potential Health HazardOngoing
Refund
Medical DeviceSeptember 7, 2018· Vital Scientific N.V.

Recalled Item: V-Twin Recalled by Vital Scientific N.V. Due to The action is being...

The Issue: The action is being initiated because the cooling indicator board was...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 7, 2018· Siemens Healthcare Diagnostics, Inc.

Recalled Item: Dimension Vista Lipase Flex Reagent Cartridge Recalled by Siemens Healthcare...

The Issue: There is lot to lot variability for QC and patient results when using the...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 7, 2018· Siemens Healthcare Diagnostics, Inc.

Recalled Item: Dimension Lipase Flex Reagent Cartridge Recalled by Siemens Healthcare...

The Issue: There is lot to lot variability for QC and patient results when using the...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 7, 2018· Bayer Medical Care, Inc.

Recalled Item: Codan Filter (Codan catalog number BC 693) used with Medrad Recalled by...

The Issue: Bayer has received reports of loose particulate in the filter when the dust...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
DrugSeptember 6, 2018· InvaGen Pharmaceuticals, Inc.

Recalled Item: Bupropion Hydrochloride ER Tablets Recalled by InvaGen Pharmaceuticals, Inc....

The Issue: Failed impurities/ degradation specifications: Out-of-specification results...

Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.

Class III — Low RiskOngoing
Refund
DrugSeptember 6, 2018· Baxter Healthcare Corporation

Recalled Item: 0.9% Sodium Chloride Injection USP 50 mL Viaflex container Baxter Recalled...

The Issue: cGMP Deviation

Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.

Class II — Potential Health HazardOngoing
Refund
DrugSeptember 6, 2018· Par Pharmaceutical, Inc.

Recalled Item: Pramipexole dihydrochloride extended release tablets Recalled by Par...

The Issue: Failed impurities/degradation specifications: Finished product contain a...

Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.

Class III — Low RiskOngoing
Refund
Medical DeviceSeptember 6, 2018· Stihler Electronic Gmbh

Recalled Item: Heating Profile PRISMAFLO II S blood return warmer for Prismaflex Recalled...

The Issue: PRISMAFLO II and PRISMAFLO II S Heating Profile only and not the Control...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 6, 2018· Stihler Electronic Gmbh

Recalled Item: Heating Profile PRISMAFLO II S blood return warmer for Prismaflex Recalled...

The Issue: PRISMAFLO II and PRISMAFLO II S Heating Profile only and not the Control...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 6, 2018· Stihler Electronic Gmbh

Recalled Item: Heating Profile PRISMAFLO II blood return warmer for Prismaflex Product...

The Issue: PRISMAFLO II and PRISMAFLO II S Heating Profile only and not the Control...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 6, 2018· Stryker Medical Division of Stryker Corporation

Recalled Item: Altrix¿ Precision Temperature Management System Model: 8001Product Usage:...

The Issue: Users may experience alarm fatigue due to frequent alarming relating to...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 6, 2018· CryoLife, Inc.

Recalled Item: CryoPatch SG Pulmonary Hemi-Artery Recalled by CryoLife, Inc. Due to The...

The Issue: The conduit length and branch length of a SG Pulmonary Hemi-Artery were...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
FoodSeptember 5, 2018· Wismettac Asian Foods (USA) dba Nishimoto Trading Co Ltd

Recalled Item: EVERYBURGER - Burger-Shaped Chocolate Cookies: NET WT. 2.32 oz. (66 Recalled...

The Issue: The ingredient list and allergen information are partially covered by a...

Recommended Action: Do not consume. Return to store for a refund or discard.

Class II — Potential Health HazardOngoing
Refund
Medical DeviceSeptember 5, 2018· Cordis Corporation

Recalled Item: Cordis POWERFLEX PRO PTA Dilatation Catheter - Product Usage: Is Recalled by...

The Issue: Product may not meet the internal manufacturing shaft subassembly burst...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 5, 2018· BioFire Diagnostics, LLC

Recalled Item: FilmArray Blood Culture Identification (BCID) Recalled by BioFire...

The Issue: Increased risk of false positive results for Proteus when the product is...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 5, 2018· Thoratec Switzerland GMBH

Recalled Item: Thoratec CentriMag Motor Recalled by Thoratec Switzerland GMBH Due to...

The Issue: Reports of circulatory support system motor stopping. Motor stop can be...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
DrugSeptember 4, 2018· Boehringer Ingelheim Pharmaceuticals, Inc.

Recalled Item: Synjardy (empagliflozin and metformin hydrochloride) Tablets. 5 mg/1000 mg....

The Issue: Cross Contamination With Other Products:

Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.

Class II — Potential Health HazardOngoing
Refund
DrugSeptember 4, 2018· Dr. Reddy's Laboratories, Inc.

Recalled Item: Tizanidine HCl Tablets Recalled by Dr. Reddy's Laboratories, Inc. Due to...

The Issue: Presence of Foreign Tablets/Capsules: Glimepiride tablet was found in a...

Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.

Class II — Potential Health HazardOngoing
Refund