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. 2,576 recalls have been distributed to Alabama in the last 12 months.

50,591 total recalls
2,576 in last 12 months

Showing 1392113940 of 28,641 recalls

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· 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· 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· Ethicon, Inc.

Recalled Item: ETHIBOND EXCEL¿ Polyester Suture-ETHIBOND Green 75cm USP1 Single Armed CT-1...

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· 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· 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· 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· 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· Philips North America, LLC

Recalled Item: SureSigns VS4 Government Bundle Recalled by Philips North America, LLC Due...

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· 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· Philips North America, LLC

Recalled Item: SureSigns VS4 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 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
Medical DeviceApril 18, 2019· Skytron, Div. The KMW Group, Inc

Recalled Item: Skytron Integrity 270 Steam Sterilizer and Skytron Integrity 270VP Steam...

The Issue: Weld attaching the air heater assembly to the main sterilizer unit has shown...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 18, 2019· Stryker Neurovascular

Recalled Item: Stryker Neurovascular Recalled by Stryker Neurovascular Due to A design...

The Issue: A design related issue can contribute to the device exhibiting brittle...

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 5502 ECC Pack Material:701051791R01 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