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. 2,348 recalls have been distributed to Alaska in the last 12 months.

46,762 total recalls
2,348 in last 12 months

Showing 2630126320 of 46,762 recalls

DrugSeptember 1, 2017· Pharmedium Services, LLC

Recalled Item: Oxytocin 40 units added to 1000 mL Lactated Ringer's USP in 1000 mL bag Rx...

The Issue: Subpotent Drug

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

Class II — Potential Health HazardOngoing
Refund
DrugSeptember 1, 2017· Pharmedium Services, LLC

Recalled Item: Oxytocin 10 units added to 500 mL Lactated Ringer's Injection USP in 500 mL...

The Issue: Subpotent Drug

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

Class II — Potential Health HazardOngoing
Refund
DrugSeptember 1, 2017· Pharmedium Services, LLC

Recalled Item: Oxytocin 10 units added to 1000 mL Lactated Ringer's Injection Recalled by...

The Issue: Subpotent Drug

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

Class II — Potential Health HazardOngoing
Refund
DrugSeptember 1, 2017· Pharmedium Services, LLC

Recalled Item: Oxytocin 20 units added to 1000 mL Lactated Ringer's Injection Recalled by...

The Issue: Subpotent Drug

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

Class II — Potential Health HazardOngoing
Refund
DrugSeptember 1, 2017· Pharmedium Services, LLC

Recalled Item: Oxytocin 30 units added to 500 mL Lactated Ringer's USP in 500 mL bag...

The Issue: Subpotent Drug

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

Class II — Potential Health HazardOngoing
Refund
DrugSeptember 1, 2017· Pharmedium Services, LLC

Recalled Item: Oxytocin 20 units added to 1000 mL Lactated Ringer's Injection Recalled by...

The Issue: Subpotent Drug

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

Class II — Potential Health HazardOngoing
Refund
DrugSeptember 1, 2017· Pharmedium Services, LLC

Recalled Item: Oxytocin 30 units added to 500 mL 5% Dextrose/Lactated Ringer's Recalled by...

The Issue: Subpotent Drug

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

Class II — Potential Health HazardOngoing
Refund
DrugSeptember 1, 2017· Pharmedium Services, LLC

Recalled Item: Oxytocin 20 units added to 1000 mL Lactated Ringer's Injection Recalled by...

The Issue: Subpotent Drug

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

Class II — Potential Health HazardOngoing
Refund
DrugSeptember 1, 2017· Pharmedium Services, LLC

Recalled Item: Oxytocin 30 units added to 500 mL Lactated Ringer's USP in 500 mL bag Rx...

The Issue: Subpotent Drug

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

Class II — Potential Health HazardOngoing
Refund
DrugSeptember 1, 2017· Pharmedium Services, LLC

Recalled Item: Oxytocin 15 units added to 250 mL Lactated Ringer's Injection USP in 250 mL...

The Issue: Subpotent Drug

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

Class II — Potential Health HazardOngoing
Refund
DrugSeptember 1, 2017· Pharmedium Services, LLC

Recalled Item: Oxytocin 40 units added to 1000 mL Lactated Ringer's USP in 1000 mL bag Rx...

The Issue: Subpotent Drug

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

Class II — Potential Health HazardOngoing
Refund
DrugSeptember 1, 2017· Pfizer Inc.

Recalled Item: Sterile Water for Injection Recalled by Pfizer Inc. Due to Non-Sterility:...

The Issue: Non-Sterility: cracked or chipped glass at the neck of Sterile Water for...

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

Class II — Potential Health HazardOngoing
Refund
Medical DeviceSeptember 1, 2017· Respire Medical

Recalled Item: Respire Pink H/S Oral Sleep Apnea Device Recalled by Respire Medical Due to...

The Issue: Potential for device breakage during use

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 1, 2017· Respire Medical

Recalled Item: Respire Pink H/S Oral Sleep Apnea Device Recalled by Respire Medical Due to...

The Issue: Potential for device breakage during use

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 1, 2017· Respire Medical

Recalled Item: Respire Pink Series EF+ Oral Sleep Apnea Device. Recalled by Respire Medical...

The Issue: Potential for device breakage during use

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 1, 2017· Respire Medical

Recalled Item: Respire Pink+ Hard/Soft Oral Sleep Apnea Device Recalled by Respire Medical...

The Issue: Potential for device breakage during use

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 1, 2017· Respire Medical

Recalled Item: Respire Pink+ Hard Oral Sleep Apnea Device Recalled by Respire Medical Due...

The Issue: Potential for device breakage during use

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 1, 2017· Aesculap Implant Systems LLC

Recalled Item: The ELAN 4 Air System is intended for high speed cutting Recalled by...

The Issue: The ELAN 4 Air System was released to the market place prior to an...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 1, 2017· Elekta Inc

Recalled Item: Elekta ERGO++ Product Usage: ERGO is often used for stereotactic treatments....

The Issue: Incorrect DICOM mapping of the exported collimator or couch angles from...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 1, 2017· Aaren Scientific Inc.

Recalled Item: AERO IOL Injection System containing 10 Z28 Cartridges per box Recalled by...

The Issue: The recommended storage temperature on the label is incorrect.

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

Class II — Potential Health HazardOngoing