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. 2,478 recalls have been distributed to Alabama in the last 12 months.

50,591 total recalls
2,478 in last 12 months

Showing 2650126520 of 50,591 recalls

Medical DeviceApril 13, 2018· St Jude Medical, Cardiac Rhythm Management Division

Recalled Item: Merlin PCS Programmer software model 3330 Recalled by St Jude Medical,...

The Issue: Devices inappropriately displayed a low battery indicator determined to be...

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

Class II — Potential Health HazardOngoing
DrugApril 13, 2018· Boiron Inc.

Recalled Item: Calendula Cream Recalled by Boiron Inc. Due to Labeling: Labeling Error on...

The Issue: Labeling: Labeling Error on Declared Strength; The outer carton (secondary...

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

Class III — Low RiskOngoing
Refund
Medical DeviceApril 13, 2018· Smiths Medical ASD Inc.

Recalled Item: Medfusion Syringe Infusion Pump Recalled by Smiths Medical ASD Inc. Due to...

The Issue: Certain Barrel Clamp Guides may contain a ridge that could potentially lead...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 13, 2018· Cardiovascular Systems Inc

Recalled Item: CSI Recalled by Cardiovascular Systems Inc Due to The pumps may switch to...

The Issue: The pumps may switch to stand-by during use requiring the pump to be reset...

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

Class II — Potential Health HazardOngoing
DrugApril 12, 2018· AMA Wholesale

Recalled Item: Rhino 69 Extreme 50000 packaged in 1 capsule per blister pack Recalled by...

The Issue: Marketed Without An Approved NDA/ANDA: FDA analysis found the product to...

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

Class I — Serious Health HazardOngoing
Refund
DrugApril 11, 2018· Premier Pharmacy Labs Inc

Recalled Item: NEOstigmine Methylsulfate (1 mg/mL) 3mg per 3mL. 3mL Single Dose Recalled by...

The Issue: Lack of Assurance of Sterility:Microbial contamination was detected during...

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

Class II — Potential Health HazardOngoing
Refund
DrugApril 11, 2018· Premier Pharmacy Labs Inc

Recalled Item: Hydromorphone HCl 1 mg/mL PF INJ. 1mL in a 3mL Recalled by Premier Pharmacy...

The Issue: Lack of Assurance of Sterility:Microbial contamination was detected during...

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

Class II — Potential Health HazardOngoing
Refund
DrugApril 11, 2018· Premier Pharmacy Labs Inc

Recalled Item: Morphine Sulfate 4 mg/mL PF Injection. 1 mL in a Recalled by Premier...

The Issue: Lack of Assurance of Sterility:Microbial contamination was detected during...

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

Class II — Potential Health HazardOngoing
Refund
DrugApril 11, 2018· Premier Pharmacy Labs Inc

Recalled Item: Morphine Sulfate 2 mg/mL PF Injection. 1 mL in a Recalled by Premier...

The Issue: Lack of Assurance of Sterility:Microbial contamination was detected during...

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

Class II — Potential Health HazardOngoing
Refund
FoodApril 11, 2018· Seabear Company

Recalled Item: Cold Smoked Wild Coho Salmon Lox Recalled by Seabear Company Due to Mislabeling

The Issue: Products recalled due to water phase salt deviations and mislabeling of...

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

Class I — Serious Health HazardOngoing
Refund
FoodApril 11, 2018· Seabear Company

Recalled Item: Hot Smoked Keta Beergarden Salmon Recalled by Seabear Company Due to Mislabeling

The Issue: Products recalled due to water phase salt deviations and mislabeling of...

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

Class I — Serious Health HazardOngoing
Refund
Medical DeviceApril 11, 2018· Arrow International Inc

Recalled Item: ARROWg+ard Blue¿ PSI Kit with Integral Hemostasis Valve/ Side Port Recalled...

The Issue: Product sterility may be compromised due to unsealed packaging.

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 11, 2018· Arrow International Inc

Recalled Item: Echogenic Introducer Needle Recalled by Arrow International Inc Due to...

The Issue: Product sterility may be compromised due to unsealed packaging.

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 11, 2018· Arrow International Inc

Recalled Item: Maximal Barrier Drape Recalled by Arrow International Inc Due to Product...

The Issue: Product sterility may be compromised due to unsealed packaging.

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 11, 2018· Arrow International Inc

Recalled Item: Pressure Injectable ARROWg+ard Blue PLUS(R) Multi-Lumen Central Venous...

The Issue: Product sterility may be compromised due to unsealed packaging.

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 11, 2018· Arrow International Inc

Recalled Item: ARROW PICC Set Recalled by Arrow International Inc Due to Product sterility...

The Issue: Product sterility may be compromised due to unsealed packaging.

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 11, 2018· Arrow International Inc

Recalled Item: Arrow-Flex(R) Percutaneous Sheath Introducer Kit with ARROWg+ard Blue(R)...

The Issue: Product sterility may be compromised due to unsealed packaging.

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 11, 2018· Arrow International Inc

Recalled Item: Arrow PICC with Chlorag+ard Technology Recalled by Arrow International Inc...

The Issue: Product sterility may be compromised due to unsealed packaging.

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 11, 2018· Arrow International Inc

Recalled Item: ARROWg+ard Blue PLUS¿ Pressure Injectable Quad-Lumen CVC Kit Recalled by...

The Issue: Product sterility may be compromised due to unsealed packaging.

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 11, 2018· Arrow International Inc

Recalled Item: Percutaneous Sheath Introducer Kit with Integral Hemostasis Valve/Side Port...

The Issue: Product sterility may be compromised due to unsealed packaging.

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

Class II — Potential Health HazardOngoing