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. 2,374 recalls have been distributed to Alaska in the last 12 months.

46,762 total recalls
2,374 in last 12 months

Showing 2168121700 of 46,762 recalls

FoodMarch 31, 2019· Wholesome Treats, Inc.

Recalled Item: Breads from Anna Yeast Free Bread Mix 18.1oz Recalled by Wholesome Treats,...

The Issue: Undeclared flaxseed. Flaxseed was used in the products but is not listed on...

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

Class III — Low RiskOngoing
Refund
FoodMarch 31, 2019· Wholesome Treats, Inc.

Recalled Item: Breads from Anna Black Bean Brownie Mix 14oz Recalled by Wholesome Treats,...

The Issue: Undeclared flaxseed. Flaxseed was used in the products but is not listed on...

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

Class III — Low RiskOngoing
Refund
Medical DeviceMarch 31, 2019· Integra Limited

Recalled Item: Integra Flowable Wound Matrix Catalog No: FWD301 Product Usage: Integra...

The Issue: Stability did not meet acceptance criteria for visual appearance during...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 30, 2019· Thoratec Corp.

Recalled Item: Thoratec Heartmate 3 Sealed Outflow Graft with Bend Relief Recalled by...

The Issue: Outflow Graft leaking at the pump connection during the implantation...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 30, 2019· Thoratec Corp.

Recalled Item: Thoratec HeartMate 3 LVAS Implant Kit Recalled by Thoratec Corp. Due to...

The Issue: Outflow Graft leaking at the pump connection during the implantation...

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

Class II — Potential Health HazardOngoing
DrugMarch 29, 2019· X-Gen Pharmaceuticals Inc.

Recalled Item: Clonidine HCL Injection Recalled by X-Gen Pharmaceuticals Inc. Due to...

The Issue: Labeling: Label Error on Declared Strength: Side carton panel incorrectly...

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

Class III — Low RiskOngoing
Refund
DrugMarch 29, 2019· Jubilant Cadista Pharmaceuticals, Inc.

Recalled Item: Pantoprazole Sodium Delayed-Release Tablets Recalled by Jubilant Cadista...

The Issue: Discoloration: Expansion of an earlier recall due to the presence of dark...

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

Class II — Potential Health HazardOngoing
Refund
Medical DeviceMarch 29, 2019· PROVIDENCE MEDICAL TECHNOLOGIES

Recalled Item: Ally Bone Screw - Product Usage:Bone Screws are indicated for Recalled by...

The Issue: There may be dimensional manufacturing error that represents a potential...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 29, 2019· GE Healthcare, LLC

Recalled Item: Prestilix 1600X Prestilix system is a fully integrated remote controlled...

The Issue: There has been a reported incident of a Distar CRT monitor that has fallen...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 29, 2019· GE Healthcare, LLC

Recalled Item: Prestige II Recalled by GE Healthcare, LLC Due to There has been a reported...

The Issue: There has been a reported incident of a Distar CRT monitor that has fallen...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 29, 2019· GE Healthcare, LLC

Recalled Item: Silhouette VR This fully integrated system offers intuitive controls with...

The Issue: There has been a reported incident of a Distar CRT monitor that has fallen...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 29, 2019· GE Healthcare, LLC

Recalled Item: Proteus XR/a The Proteus XR/a radiographic system offers the flexibility...

The Issue: There has been a reported incident of a Distar CRT monitor that has fallen...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 29, 2019· Conformis, Inc.

Recalled Item: Conformis iTotal Hip Replacement System: HBS-033-00xx-010101 Recalled by...

The Issue: Discrepancy of 3mm between the values displayed and approved by surgeons in...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 29, 2019· Conformis, Inc.

Recalled Item: Conformis iTotal Hip Replacement System: HBS-033-00xx-020101 Recalled by...

The Issue: Discrepancy of 3mm between the values displayed and approved by surgeons in...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 29, 2019· GE Healthcare, LLC

Recalled Item: Precision 500D The Precision 500D R&F X-ray System is intended Recalled by...

The Issue: There has been a reported incident of a Distar CRT monitor that has fallen...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 29, 2019· Centurion Medical Products Corporation

Recalled Item: Sterile Nail Clipper Concave Edge (67710) Recalled by Centurion Medical...

The Issue: Compromised seal on the sterile barrier pouch.

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 29, 2019· Centurion Medical Products Corporation

Recalled Item: Sterile Nail Nipper Recalled by Centurion Medical Products Corporation Due...

The Issue: Compromised seal on the sterile barrier pouch.

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 28, 2019· Philips North America, LLC

Recalled Item: IntelliVue MX40 Patient Monitor Recalled by Philips North America, LLC Due...

The Issue: The MX40 may experience increased power consumption and may have a lack of...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 28, 2019· Philips North America, LLC

Recalled Item: IntelliVue MX40 Patient Monitor Recalled by Philips North America, LLC Due...

The Issue: The MX40 may experience increased power consumption and may have a lack of...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 28, 2019· Philips North America, LLC

Recalled Item: IntelliVue MX40 Patient Monitor Recalled by Philips North America, LLC Due...

The Issue: The MX40 may experience increased power consumption and may have a lack of...

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

Class II — Potential Health HazardOngoing