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 2678126800 of 50,591 recalls

FoodMarch 16, 2018· Natural Grocers by Vitamin Cottage

Recalled Item: Natural Grocers Organic Coconut Smiles Recalled by Natural Grocers by...

The Issue: Coconut smiles product tested positive for Salmonella.

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

Class I — Serious Health HazardOngoing
Refund
FoodMarch 16, 2018· NGB, Corp

Recalled Item: Nxtgen Botanicals Recalled by NGB, Corp Due to Potential Salmonella...

The Issue: NGB Corp is recalling Nxtgen Botanicals due to potential Salmonella...

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

Class I — Serious Health HazardOngoing
Refund
FoodMarch 16, 2018· Smucker Natural Foods, Inc.

Recalled Item: SANTA CRUZ organic MANGO fruit spread NET WT 9.5 OZ Recalled by Smucker...

The Issue: The firm was notified that the product did not have an ingredient panel or...

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

Class III — Low RiskOngoing
Refund
FoodMarch 16, 2018· Smucker Natural Foods, Inc.

Recalled Item: SANTA CRUZ organic SEEDLESS RED RASPBERRY fruit spread NET WT Recalled by...

The Issue: The firm was notified that the product did not have an ingredient panel or...

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

Class III — Low RiskOngoing
Refund
FoodMarch 16, 2018· Smucker Natural Foods, Inc.

Recalled Item: SANTA CRUZ organic STRAWBERRY fruit spread NET WT 9.5 OZ Recalled by Smucker...

The Issue: The firm was notified that the product did not have an ingredient panel or...

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

Class III — Low RiskOngoing
Refund
Medical DeviceMarch 16, 2018· Philips Electronics North America Corporation

Recalled Item: Intera 1.0T Recalled by Philips Electronics North America Corporation Due to...

The Issue: Potential risk for helium gas inside the MR examination room during a magnet...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 16, 2018· Philips Electronics North America Corporation

Recalled Item: Conversion SmarthPath to dStream for 1.5T Recalled by Philips Electronics...

The Issue: Potential risk for helium gas inside the MR examination room during a magnet...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 16, 2018· Philips Electronics North America Corporation

Recalled Item: T5-NT Recalled by Philips Electronics North America Corporation Due to...

The Issue: Potential risk for helium gas inside the MR examination room during a magnet...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 16, 2018· Philips Electronics North America Corporation

Recalled Item: Intera 0.5T Standard Recalled by Philips Electronics North America...

The Issue: Potential risk for helium gas inside the MR examination room during a magnet...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 16, 2018· Terumo Cardiovascular Systems Corporation

Recalled Item: Sarns TCM II Recalled by Terumo Cardiovascular Systems Corporation Due to...

The Issue: Update to cooler-heater cleaning instructions.

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 16, 2018· Philips Electronics North America Corporation

Recalled Item: Panorama 1.0T Recalled by Philips Electronics North America Corporation Due...

The Issue: Potential risk for helium gas inside the MR examination room during a magnet...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 16, 2018· Terumo Cardiovascular Systems Corporation

Recalled Item: Terumo HX2 Temperature Management System Recalled by Terumo Cardiovascular...

The Issue: Update to cooler-heater cleaning instructions.

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 16, 2018· Terumo Cardiovascular Systems Corporation

Recalled Item: Sarns TCM Recalled by Terumo Cardiovascular Systems Corporation Due to...

The Issue: Update to cooler-heater cleaning instructions.

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 16, 2018· Philips Electronics North America Corporation

Recalled Item: Ingenia 1.5T CX Recalled by Philips Electronics North America Corporation...

The Issue: Potential risk for helium gas inside the MR examination room during a magnet...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 16, 2018· Philips Electronics North America Corporation

Recalled Item: Multiva systems Recalled by Philips Electronics North America Corporation...

The Issue: Potential risk for helium gas inside the MR examination room during a magnet...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 16, 2018· Philips Electronics North America Corporation

Recalled Item: Multiva systems Recalled by Philips Electronics North America Corporation...

The Issue: Potential risk for helium gas inside the MR examination room during a magnet...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 16, 2018· Philips Electronics North America Corporation

Recalled Item: T10-NT Recalled by Philips Electronics North America Corporation Due to...

The Issue: Potential risk for helium gas inside the MR examination room during a magnet...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 16, 2018· GE Medical Systems Ultrasound & Primary Care Diagnostics, LL

Recalled Item: GE Healthcare Lunar: a) DPX Duo Recalled by GE Medical Systems Ultrasound &...

The Issue: Under certain conditions, when using DICOM Worklist along with DICOM MPPS, a...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 16, 2018· Philips Electronics North America Corporation

Recalled Item: ACS-NT Recalled by Philips Electronics North America Corporation Due to...

The Issue: Potential risk for helium gas inside the MR examination room during a magnet...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 16, 2018· Philips Electronics North America Corporation

Recalled Item: Achieva 1.5T: 1) Nova (Dual) Recalled by Philips Electronics North America...

The Issue: Potential risk for helium gas inside the MR examination room during a magnet...

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

Class II — Potential Health HazardOngoing