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. 2,448 recalls have been distributed to Alabama in the last 12 months.

50,591 total recalls
2,448 in last 12 months

Showing 3576135780 of 50,591 recalls

Medical DeviceJanuary 4, 2016· Otto Bock Healthcare GmbH

Recalled Item: Ottobock Modular Polycentric EBS Knee Joint 3R60 Recalled by Otto Bock...

The Issue: Otto Bock HealthCare GmbH is recalling Modular Polycentric EBS Knee Joint...

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

Class II — Potential Health HazardOngoing
DrugDecember 31, 2015· Pharmedium Services, LLC

Recalled Item: NORepinephrine Bitartrate Recalled by Pharmedium Services, LLC Due to...

The Issue: Subpotent Drug; confirmed results by FDA analysis after customer complaints...

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

Class III — Low RiskOngoing
Refund
DrugDecember 31, 2015· Pharmedium Services, LLC

Recalled Item: NORepinephrine Bitartrate Recalled by Pharmedium Services, LLC Due to...

The Issue: Subpotent Drug; confirmed results by FDA analysis after customer complaints...

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

Class III — Low RiskOngoing
Refund
DrugDecember 31, 2015· Sandoz Inc

Recalled Item: Candesartan Cilexetil Tablets Recalled by Sandoz Inc Due to Failed...

The Issue: Failed Impurities/Degradation Specifications; 9 month stability timepoint

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

Class III — Low RiskOngoing
Refund
Medical DeviceDecember 31, 2015· Cordis Corporation

Recalled Item: CORDIS AVANTI + CATHETER SHEATH INTRODUCER SYSTEM The product includes...

The Issue: Incorrect cannula of the sheath introducer (smaller than intended).

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 29, 2015· Pharmacaribe llc

Recalled Item: PharmaCaribe PulmoSal 7% Sodium chloride Recalled by Pharmacaribe llc Due to...

The Issue: Vials were labeled as USP 7% Hypertonic saline instead of PulmoSal 7% (pH+)

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 29, 2015· Radiometer America Inc

Recalled Item: AQURE System Recalled by Radiometer America Inc Due to The AQURE System has...

The Issue: The AQURE System has a design error regarding sample type in which sample...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 29, 2015· Siemens Healthcare Diagnostics, Inc

Recalled Item: ADVIA Centaur PSA Assay Recalled by Siemens Healthcare Diagnostics, Inc Due...

The Issue: PSA assay is not meeting the High Dose Hook Effect expectation in the...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 28, 2015· Phadia Ab

Recalled Item: EliA SmDP Well Recalled by Phadia Ab Due to All equivocal and positive...

The Issue: All equivocal and positive results (greater or equal 7 EliA U/ml) on EliA...

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

Class II — Potential Health HazardOngoing
DrugDecember 24, 2015· Macleods Pharma Usa Inc

Recalled Item: Pramipexole Dihydrochloride Tablets 0.125 mg Recalled by Macleods Pharma Usa...

The Issue: Presence of Foreign Tablets/Capsules: Presence of a comingled Carbimazole 5...

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

Class II — Potential Health HazardOngoing
Refund
DrugDecember 23, 2015· Nuway Distributors, LLC

Recalled Item: APEXXX tablets Recalled by Nuway Distributors, LLC Due to Marketed Without...

The Issue: Marketed Without An Approved NDA/ANDA: tainted product marketed as a dietary...

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

Class I — Serious Health HazardOngoing
Refund
FoodDecember 23, 2015· Milky Way Intl Trading Corp

Recalled Item: Mandarin Oranges (In Light Syrup) Recalled by Milky Way Intl Trading Corp...

The Issue: MW Polar Foods is recalling Mandarin Oranges due to possible glass in product.

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

Class II — Potential Health HazardOngoing
Refund
Medical DeviceDecember 23, 2015· Cardinal Scale Mfg Co

Recalled Item: Cardinal Recalled by Cardinal Scale Mfg Co Due to One complaint of a seat on...

The Issue: One complaint of a seat on a scale failing unexpectedly which can cause an...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 23, 2015· Fujifilm Medical Systems U.S.A., Inc.

Recalled Item: Endoscope ED-250XL5 Operations Manual: Cleaning Recalled by Fujifilm Medical...

The Issue: This correction is in response to publicized reports of multi-drug resistant...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 23, 2015· Fujifilm Medical Systems U.S.A., Inc.

Recalled Item: Endoscope ED-450XL5 Operation Manual: Cleaning Recalled by Fujifilm Medical...

The Issue: This correction is in response to publicized reports of multi-drug resistant...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 23, 2015· Fujifilm Medical Systems U.S.A., Inc.

Recalled Item: Endoscope ED-250XT5 Operations Manual: Cleaning Disinfection and Storage...

The Issue: This correction is in response to publicized reports of multi-drug resistant...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 23, 2015· Fujifilm Medical Systems U.S.A., Inc.

Recalled Item: Endoscope Recalled by Fujifilm Medical Systems U.S.A., Inc. Due to This...

The Issue: This correction is in response to publicized reports of multi-drug resistant...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 23, 2015· Fujifilm Medical Systems U.S.A., Inc.

Recalled Item: Endoscope ED-450XT5 Operation Manual: Cleaning Recalled by Fujifilm Medical...

The Issue: This correction is in response to publicized reports of multi-drug resistant...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 23, 2015· Xeridiem Mediem Medical Devices Inc

Recalled Item: EndoVive 3s Low Profile Balloon Kits Part Number: M00549470 (XMD Recalled by...

The Issue: A feeding () valve leakage issue. The feeding valve appears to close...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 23, 2015· Xeridiem Mediem Medical Devices Inc

Recalled Item: EndoVive 3s Low Profile Balloon Kits Part Number: M00549530 (XMD Recalled by...

The Issue: A feeding () valve leakage issue. The feeding valve appears to close...

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

Class II — Potential Health HazardOngoing