Product Recalls in Alaska

Product recalls affecting Alaska — including food, drugs, consumer products, medical devices, and vehicles distributed to Alaska. RecallDetector monitors distribution data from the FDA, USDA, CPSC, and NHTSA to show you which recalls are relevant to your area. 2,384 recalls have been distributed to Alaska in the last 12 months.

46,762 total recalls
2,384 in last 12 months

Showing 2032120340 of 46,762 recalls

FoodJuly 9, 2019· Probar LLC

Recalled Item: PROBAR The Simply Real Bar: Chocolate Coconut Recalled by Probar LLC Due to...

The Issue: Chocolate chip containing meal bars potentially contain undeclared milk and soy

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

Class I — Serious Health HazardOngoing
Refund
FoodJuly 9, 2019· Probar LLC

Recalled Item: PROBAR MEAL Superfood Slam Recalled by Probar LLC Due to Undeclared Milk

The Issue: Chocolate chip containing meal bars potentially contain undeclared milk and soy

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

Class I — Serious Health HazardOngoing
Refund
DrugJuly 9, 2019· Jubilant Cadista Pharmaceuticals, Inc.

Recalled Item: Drospirenone and Ethinyl Estradiol Tablets Recalled by Jubilant Cadista...

The Issue: Failed dissolution specifications : failed results at the 3-month stability...

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

Class I — Serious Health HazardOngoing
Refund
DrugJuly 8, 2019· Piramal Critical Care, Inc.

Recalled Item: Gablofen (baclofen injection) Recalled by Piramal Critical Care, Inc. Due to...

The Issue: Failed Impurities/Degradation Specification -This recall is being initiated...

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

Class II — Potential Health HazardOngoing
Refund
Medical DeviceJuly 8, 2019· Ortho Clinical Diagnostics

Recalled Item: VITROS 4600 Chemistry System Recalled by Ortho Clinical Diagnostics Due to...

The Issue: Potential Unsuccessful Calibration Due to Software Anomaly in VITROS System

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 8, 2019· Ortho Clinical Diagnostics

Recalled Item: VITROS 5600 Integrated System Recalled by Ortho Clinical Diagnostics Due to...

The Issue: Potential Unsuccessful Calibration Due to Software Anomaly in VITROS System

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 8, 2019· Ortho Clinical Diagnostics

Recalled Item: VITROS 5 Recalled by Ortho Clinical Diagnostics Due to Potential...

The Issue: Potential Unsuccessful Calibration Due to Software Anomaly in VITROS System

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 8, 2019· Ortho Clinical Diagnostics

Recalled Item: VITROS 350 Chemistry System Recalled by Ortho Clinical Diagnostics Due to...

The Issue: Potential Unsuccessful Calibration Due to Software Anomaly in VITROS System

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 8, 2019· Ortho Clinical Diagnostics

Recalled Item: VITROS 5600 Integrated System Recalled by Ortho Clinical Diagnostics Due to...

The Issue: Potential Unsuccessful Calibration Due to Software Anomaly in VITROS System

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 8, 2019· CooperSurgical, Inc.

Recalled Item: TransWarmer Warming Infant Transport Mattress Recalled by CooperSurgical,...

The Issue: The firm updated the IFU in April 2019 to clarify that use of the...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 8, 2019· Ortho Clinical Diagnostics

Recalled Item: VITROS Chemistry Products Calibrator Kit 32 Recalled by Ortho Clinical...

The Issue: Potential Unsuccessful Calibration Due to Software Anomaly in VITROS System

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 8, 2019· Ortho Clinical Diagnostics

Recalled Item: VITROS 250AT Chemistry System Recalled by Ortho Clinical Diagnostics Due to...

The Issue: Potential Unsuccessful Calibration Due to Software Anomaly in VITROS System

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 8, 2019· Ortho Clinical Diagnostics

Recalled Item: VITROS 4600 Chemistry System Recalled by Ortho Clinical Diagnostics Due to...

The Issue: Potential Unsuccessful Calibration Due to Software Anomaly in VITROS System

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 8, 2019· Ortho Clinical Diagnostics

Recalled Item: VITROS Chemistry Products Calibrator Kit 32 Recalled by Ortho Clinical...

The Issue: Potential Unsuccessful Calibration Due to Software Anomaly in VITROS System

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 8, 2019· Ortho Clinical Diagnostics

Recalled Item: VITROS 5 Recalled by Ortho Clinical Diagnostics Due to Potential...

The Issue: Potential Unsuccessful Calibration Due to Software Anomaly in VITROS System

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 8, 2019· Ortho Clinical Diagnostics

Recalled Item: VITROS 250 Chemistry System Recalled by Ortho Clinical Diagnostics Due to...

The Issue: Potential Unsuccessful Calibration Due to Software Anomaly in VITROS System

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 8, 2019· Smiths Medical ASD Inc.

Recalled Item: GRIPPER Needles sold as part of PORT-A-CATH II SINGLE LUMEN Recalled by...

The Issue: Potential for certain GRIPPER Needles to contain an occluded or blocked needle.

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 8, 2019· Ortho Clinical Diagnostics

Recalled Item: VITROS 250 Chemistry System Recalled by Ortho Clinical Diagnostics Due to...

The Issue: Potential Unsuccessful Calibration Due to Software Anomaly in VITROS System

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 8, 2019· Smiths Medical ASD Inc.

Recalled Item: GRIPPER Needles sold individually. Labeled as the following item...

The Issue: Potential for certain GRIPPER Needles to contain an occluded or blocked needle.

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 8, 2019· Becton, Dickinson and Company, BD Biosciences

Recalled Item: BD FACS Sample Prep Assistant (SPA) II - Product Usage: Recalled by Becton,...

The Issue: The recalling firm confirmed that BD FACS Sample Prep Assistant (SPA) II and...

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

Class II — Potential Health HazardOngoing