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. 2,299 recalls have been distributed to Alaska in the last 12 months.

46,762 total recalls
2,299 in last 12 months

Showing 3916139180 of 46,762 recalls

Medical DeviceJuly 7, 2014· Smiths Medical ASD, Inc.

Recalled Item: 4001PS Neonatal/Paed.Intubation Kit 2.5mm Murphy Recalled by Smiths Medical...

The Issue: The tube fastener on the ET Tube Holder may compress the tracheal tube when...

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

Class I — Serious Health HazardOngoing
Medical DeviceJuly 7, 2014· Smiths Medical ASD, Inc.

Recalled Item: H4002PS Neonatal/Paed.Intubation Kit 3.0mm Murphy Recalled by Smiths Medical...

The Issue: The tube fastener on the ET Tube Holder may compress the tracheal tube when...

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

Class I — Serious Health HazardOngoing
Medical DeviceJuly 3, 2014· Intelerad Medical Systems

Recalled Item: IntelePACS software versions 3-8-1 to 4-9-1 Recalled by Intelerad Medical...

The Issue: In specific situation a partially truncated file may be written to the...

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

Class II — Potential Health HazardOngoing
DrugJuly 3, 2014· Fougera Pharmaceuticals Inc.

Recalled Item: Triamcinolone Acetonide Lotion USP Recalled by Fougera Pharmaceuticals Inc....

The Issue: Failed PH Specifications: It has been determined that the pH of the lots...

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

Class III — Low RiskOngoing
Refund
DrugJuly 3, 2014· Mylan Pharmaceuticals Inc.

Recalled Item: Metoprolol Succinate Extended-release Tablets Recalled by Mylan...

The Issue: Presence of Foreign Tablets/Capsules: A pharmacist reported a rogue tablet...

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

Class II — Potential Health HazardOngoing
Refund
DrugJuly 3, 2014· Mylan Institutional, Inc. (d.b.a. UDL Laboratories)

Recalled Item: Diltiazem HCl Extended-release Capsules Recalled by Mylan Institutional,...

The Issue: Failed Impurities/Degradation Specifications: High out-of-specification...

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

Class III — Low RiskOngoing
Refund
DrugJuly 3, 2014· Fougera Pharmaceuticals Inc.

Recalled Item: Triamcinolone Acetonide Lotion USP Recalled by Fougera Pharmaceuticals Inc....

The Issue: Failed PH Specifications: It has been determined that the pH of the lots...

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

Class III — Low RiskOngoing
Refund
FoodJuly 3, 2014· Metagenics, Inc.

Recalled Item: UltraBalance Protein Powder Recalled by Metagenics, Inc. Due to Undeclared Soy

The Issue: Metagenics is recalling UltraBalance Protein powder because it may contain...

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

Class II — Potential Health HazardOngoing
Refund
Medical DeviceJuly 2, 2014· Smith & Nephew, Inc.

Recalled Item: TRIGEN(R) INTERTAN(TM) 10MM X 18 CM NAIL Recalled by Smith & Nephew, Inc....

The Issue: There was an error in manufacturing which resulted in the proximal lag screw...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 2, 2014· Hospira Inc.

Recalled Item: The Plum A+ Infusion System is designed to meet the Recalled by Hospira Inc....

The Issue: One lot of alarm assemblies used in Plum A+ and Plum A+3 infusion pumps may...

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

Class I — Serious Health HazardOngoing
Medical DeviceJuly 2, 2014· Hospira Inc.

Recalled Item: The Plum A+ Infusion System is designed to meet the Recalled by Hospira Inc....

The Issue: One lot of alarm assemblies used in Plum A+ and Plum A+3 infusion pumps may...

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

Class I — Serious Health HazardOngoing
Medical DeviceJuly 2, 2014· Hospira Inc.

Recalled Item: The Plum A+ Infusion System is designed to meet the Recalled by Hospira Inc....

The Issue: One lot of alarm assemblies used in Plum A+ and Plum A+3 infusion pumps may...

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

Class I — Serious Health HazardOngoing
Medical DeviceJuly 2, 2014· Mentor Texas, LP.

Recalled Item: EN MENTOR Round High Profile Single Use Saline Breast Implant Recalled by...

The Issue: The device labeling is stamped with 330cc and the device is actually 380cc...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 2, 2014· Hospira Inc.

Recalled Item: The Plum A+ Infusion System is designed to meet the Recalled by Hospira Inc....

The Issue: One lot of alarm assemblies used in Plum A+ and Plum A+3 infusion pumps may...

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

Class I — Serious Health HazardOngoing
Medical DeviceJuly 2, 2014· Hospira Inc.

Recalled Item: The Plum A+ Infusion System is designed to meet the Recalled by Hospira Inc....

The Issue: One lot of alarm assemblies used in Plum A+ and Plum A+3 infusion pumps may...

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

Class I — Serious Health HazardOngoing
DrugJuly 2, 2014· Bracco Diagnostic Inc

Recalled Item: E-Z-HD (barium sulfate) For Suspension (98% w/w) Recalled by Bracco...

The Issue: Subpotent Drug: Low out of specification results for both pH and assay...

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

Class III — Low RiskOngoing
Refund
DrugJuly 1, 2014· American Health Packaging

Recalled Item: Oxcarbazepine Tablets Recalled by American Health Packaging Due to Labeling:...

The Issue: Labeling: Label Mix-Up: Some cartons of AHP Ibuprofen Tablets, USP, 600mg,...

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

Class I — Serious Health HazardOngoing
Refund
DrugJuly 1, 2014· American Health Packaging

Recalled Item: Ibuprofen Tablets Recalled by American Health Packaging Due to Labeling:...

The Issue: Labeling: Label Mix-Up: Some cartons of AHP Ibuprofen Tablets, USP, 600mg,...

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

Class I — Serious Health HazardOngoing
Refund
FoodJuly 1, 2014· PUREFRUIT CHILE S.A

Recalled Item: HyVee applesauce Recalled by PUREFRUIT CHILE S.A Due to Purefruit Chile S.A....

The Issue: Purefruit Chile S.A. is recalling pouched applesauce due to the possibility...

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

Class II — Potential Health HazardOngoing
Refund
FoodJuly 1, 2014· PUREFRUIT CHILE S.A

Recalled Item: Market Pantry Apple Recalled by PUREFRUIT CHILE S.A Due to Purefruit Chile...

The Issue: Purefruit Chile S.A. is recalling pouched applesauce due to the possibility...

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

Class II — Potential Health HazardOngoing
Refund