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. 2,508 recalls have been distributed to Alabama in the last 12 months.

50,591 total recalls
2,508 in last 12 months

Showing 2260122620 of 50,591 recalls

Medical DeviceApril 19, 2019· AURIS HEALTH INC

Recalled Item: Monarch Recalled by AURIS HEALTH INC Due to Reports of aspirating biopsy...

The Issue: Reports of aspirating biopsy needle breakage

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 19, 2019· Isopure Corp

Recalled Item: Finish Thompson Centrifugal Pump Model #110192-3 (sold as spare part)...

The Issue: There is a potential for an uneven plastic encapsulation of the magnet ring...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 19, 2019· Isopure Corp

Recalled Item: Isopure Sodium Bicarbonate Mixing and Distribution System (IsoMix PRO) with...

The Issue: There is a potential for an uneven plastic encapsulation of the magnet ring...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 19, 2019· Philips North America, LLC

Recalled Item: SureSigns VS3 NBP Temp Recalled by Philips North America, LLC Due to System...

The Issue: System software inhibits the monitor and as a result does not measure,...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 19, 2019· Philips North America, LLC

Recalled Item: SureSigns VS3 NBP Recalled by Philips North America, LLC Due to System...

The Issue: System software inhibits the monitor and as a result does not measure,...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 19, 2019· Ethicon, Inc.

Recalled Item: ETHIBOND EXCEL ETHIBOND Polvester Suture-Green 75cm USP1 Single Armed CTX...

The Issue: Possibility that a suture raw material containing high endotoxin levels was...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 19, 2019· Isopure Corp

Recalled Item: Acidified Concentrate Distribution and Storage System (ACDS System) with a...

The Issue: There is a potential for an uneven plastic encapsulation of the magnet ring...

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

Class II — Potential Health HazardOngoing
DrugApril 19, 2019· Alvogen, Inc

Recalled Item: FENTANYL Transdermal System Recalled by Alvogen, Inc Due to Product Mix-Up:...

The Issue: Product Mix-Up: Customer complaint that their carton labeled as Fentanyl...

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

Class I — Serious Health HazardOngoing
Refund
DrugApril 19, 2019· Pacifico National, Inc. dba AmEx Pharmacy

Recalled Item: BEVACIZUMAB 1.25 mg/0.05 mL 31G MJ syringe Intravitreal Injection. This...

The Issue: Defective Delivery System: difficult to express

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

Class II — Potential Health HazardOngoing
Refund
DrugApril 18, 2019· Torrent Pharma Inc.

Recalled Item: Losartan Potassium Tablets Recalled by Torrent Pharma Inc. Due to CGMP...

The Issue: CGMP Deviations: FDA lab confirmed presence of an impurity,...

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

Class II — Potential Health HazardOngoing
Refund
DrugApril 18, 2019· Torrent Pharma Inc.

Recalled Item: Losartan Potassium and Hydrochlorothiazide Tablets Recalled by Torrent...

The Issue: CGMP Deviations: FDA lab confirmed presence of an impurity,...

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

Class II — Potential Health HazardOngoing
Refund
DrugApril 18, 2019· Torrent Pharma Inc.

Recalled Item: Losartan Potassium Tablets Recalled by Torrent Pharma Inc. Due to CGMP...

The Issue: CGMP Deviations: FDA lab confirmed presence of an impurity,...

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

Class II — Potential Health HazardOngoing
Refund
DrugApril 18, 2019· Torrent Pharma Inc.

Recalled Item: Losartan Potassium and Hydrochlorothiazide Tablets Recalled by Torrent...

The Issue: CGMP Deviations: FDA lab confirmed presence of an impurity,...

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

Class II — Potential Health HazardOngoing
Refund
DrugApril 18, 2019· Torrent Pharma Inc.

Recalled Item: Losartan Potassium and Hydrochlorothiazide Tablets Recalled by Torrent...

The Issue: CGMP Deviations: FDA lab confirmed presence of an impurity,...

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

Class II — Potential Health HazardOngoing
Refund
DrugApril 18, 2019· Torrent Pharma Inc.

Recalled Item: Losartan Potassium Tablets Recalled by Torrent Pharma Inc. Due to CGMP...

The Issue: CGMP Deviations: FDA lab confirmed presence of an impurity,...

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

Class II — Potential Health HazardOngoing
Refund
Medical DeviceApril 18, 2019· Maquet Cardiovascular, LLC

Recalled Item: Maquet Getinge- BEQ-T 39700 ECC Pack Material:701062473R01 Recalled by...

The Issue: Custom Tubing Sets for Extracorporeal Circulation (ECC)-During...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 18, 2019· Maquet Cardiovascular, LLC

Recalled Item: Maquet Getinge-BEQ-T 8805 ECC PACK Material: 701053361 Recalled by Maquet...

The Issue: Custom Tubing Sets for Extracorporeal Circulation (ECC)-During...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 18, 2019· Maquet Cardiovascular, LLC

Recalled Item: Maquet Getinge-BEQ-TOP 33704 ECC 1/4" PACK Material: 701054150 Recalled by...

The Issue: Custom Tubing Sets for Extracorporeal Circulation (ECC)-During...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 18, 2019· Maquet Cardiovascular, LLC

Recalled Item: Maquet Getinge-T 8030 4 in High Flow Pigtail Material: 709000366 Recalled by...

The Issue: Custom Tubing Sets for Extracorporeal Circulation (ECC)-During...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 18, 2019· Maquet Cardiovascular, LLC

Recalled Item: Maquet Getinge-BEQ-TOP 27901 SMALL PATIENT CI Material:701052287 Recalled by...

The Issue: Custom Tubing Sets for Extracorporeal Circulation (ECC)-During...

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

Class II — Potential Health HazardOngoing