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.

50,591 total recalls
2,467 in last 12 months

Showing 3062130640 of 50,591 recalls

FoodApril 14, 2017· Kemps, LLC

Recalled Item: Kemps Sweet Me Creamery Expresso Mocha Recalled by Kemps, LLC Due to Kemps...

The Issue: Kemps is recalling select pints of Sweet Me Creamery Ice Cream and YO2...

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

Class II — Potential Health HazardOngoing
Refund
FoodApril 14, 2017· Kemps, LLC

Recalled Item: Kemps Sweet Me Creamery Vanilla Bean Recalled by Kemps, LLC Due to Kemps is...

The Issue: Kemps is recalling select pints of Sweet Me Creamery Ice Cream and YO2...

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

Class II — Potential Health HazardOngoing
Refund
FoodApril 14, 2017· Kemps, LLC

Recalled Item: Kemps YO2 Frozen Yogurt Chocolate Peanut Butter Fudge Recalled by Kemps, LLC...

The Issue: Kemps is recalling select pints of Sweet Me Creamery Ice Cream and YO2...

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

Class II — Potential Health HazardOngoing
Refund
FoodApril 13, 2017· General Mills, Inc

Recalled Item: Chocolate chip cookie dough larabars Recalled by General Mills, Inc Due to...

The Issue: Chocolate chip cookie dough larabars which contain cashews were incorrectly...

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

Class II — Potential Health HazardOngoing
Refund
Medical DeviceApril 13, 2017· Pentax of America Inc

Recalled Item: 9310HD Digital Video Capture Modules Product Usage: The 9310HD is Recalled...

The Issue: Pentax Medical did not always provide transformers with 9175 isolation...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 13, 2017· BioMerieux SA

Recalled Item: ETEST OXACILLIN OX 256 US F100 In vitro diagnostic Recalled by BioMerieux SA...

The Issue: QC failures (MIC out of range high) for S.aureus ATCC 29213 strain on ETEST...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 13, 2017· Pentax of America Inc

Recalled Item: 7245C Recalled by Pentax of America Inc Due to Pentax Medical did not always...

The Issue: Pentax Medical did not always provide transformers with 9175 isolation...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 13, 2017· BioMerieux SA

Recalled Item: ETEST OXACILLIN OX 256 WW F100 In vitro diagnostic Recalled by BioMerieux SA...

The Issue: QC failures (MIC out of range high) for S.aureus ATCC 29213 strain on ETEST...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 13, 2017· CardioTek BV

Recalled Item: CardioTek EP-TRACER Software V1.x and V2.0 The EP-TRACER System is Recalled...

The Issue: Software bug which allows parameters to be changed unintentionally during use.

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 13, 2017· Pentax of America Inc

Recalled Item: 9200C and 9200D Laryngeal Strobe Product Usage: The 9310HD is Recalled by...

The Issue: Pentax Medical did not always provide transformers with 9175 isolation...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 13, 2017· Pentax of America Inc

Recalled Item: 9400 Laryngeal Strobe Product Usage: The 9310HD is used to Recalled by...

The Issue: Pentax Medical did not always provide transformers with 9175 isolation...

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

Class II — Potential Health HazardOngoing
DrugApril 13, 2017· Spectrum Laboratory Products, Inc.

Recalled Item: Levonorgestrel Recalled by Spectrum Laboratory Products, Inc. Due to CGMP...

The Issue: CGMP Deviations: these repackaged and redistributed products are being...

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

Class II — Potential Health HazardOngoing
Refund
DrugApril 13, 2017· Spectrum Laboratory Products, Inc.

Recalled Item: Estradiol (17-B-Estradiol Recalled by Spectrum Laboratory Products, Inc. Due...

The Issue: CGMP Deviations: these repackaged and redistributed products are being...

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

Class II — Potential Health HazardOngoing
Refund
DrugApril 13, 2017· Standard Homeopathic Company

Recalled Item: Hyland's Baby Nighttime Teething Tablets [Belladonna 12X HPUS...

The Issue: Superpotent Drug: FDA analysis found inconsistent amounts of belladonna...

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

Class I — Serious Health HazardOngoing
Refund
DrugApril 13, 2017· Standard Homeopathic Company

Recalled Item: Hyland's Baby Teething Tablets [Calcarea Phosporica 6X HPUS Recalled by...

The Issue: Superpotent Drug: FDA analysis found inconsistent amounts of belladonna...

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

Class I — Serious Health HazardOngoing
Refund
Medical DeviceApril 12, 2017· Datascope Corporation

Recalled Item: SENSATION PLUS¿ 8Fr. 50cc Intra-Aortic Balloon Catheter with Insertion Kit...

The Issue: Maquet/Getinge is initiating a voluntary product removal involving four lot...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 12, 2017· XTANT MEDICAL INC

Recalled Item: 5.5mm Diameter x 500mm CoCr Straight Rod Recalled by XTANT MEDICAL INC Due...

The Issue: The material type on the label may incorrectly state Ti6Al-4V ELI. The...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 12, 2017· Siemens Medical Solutions USA, Inc

Recalled Item: AXIOM Sensis Recalled by Siemens Medical Solutions USA, Inc Due to An...

The Issue: An extremely dusty computer can cause problems at system start, or rarely,...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 12, 2017· Medtronic Inc., Cardiac Rhythm and Heart Failure

Recalled Item: Amplia MRI Quad CRT-0 SureScan Claria MRI Quad CRT-D SureScan Recalled by...

The Issue: An unexpected transient mode switch behavior was detected by Medtronic...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 11, 2017· Sorin Group Italia SRL - CRF

Recalled Item: PARADYM Models: VR 8250 Recalled by Sorin Group Italia SRL - CRF Due to...

The Issue: Sorin is notifying physicians that certain defibrillators' battery depletion...

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

Class II — Potential Health HazardOngoing