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. 2,440 recalls have been distributed to Alaska in the last 12 months.

46,762 total recalls
2,440 in last 12 months

Showing 1742117440 of 46,762 recalls

Medical DeviceJune 16, 2020· CME America, LLC

Recalled Item: CMExpress Microbore Sets Recalled by CME America, LLC Due to Infusion...

The Issue: Infusion administration sets may have a delivery inaccuracy over plus/minus...

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

Class I — Serious Health HazardOngoing
Medical DeviceJune 16, 2020· CME America, LLC

Recalled Item: CMExpress Microbore Sets Recalled by CME America, LLC Due to Infusion...

The Issue: Infusion administration sets may have a delivery inaccuracy over plus/minus...

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

Class I — Serious Health HazardOngoing
Medical DeviceJune 16, 2020· CME America, LLC

Recalled Item: BodyGuard Microset Recalled by CME America, LLC Due to Infusion...

The Issue: Infusion administration sets may have a delivery inaccuracy over plus/minus...

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

Class I — Serious Health HazardOngoing
Medical DeviceJune 16, 2020· CME America, LLC

Recalled Item: BodyGuard Microset Recalled by CME America, LLC Due to Infusion...

The Issue: Infusion administration sets may have a delivery inaccuracy over plus/minus...

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

Class I — Serious Health HazardOngoing
Medical DeviceJune 16, 2020· CME America, LLC

Recalled Item: BodyGuard Microset w/ Non-Vented Spike Connector Recalled by CME America,...

The Issue: Infusion administration sets may have a delivery inaccuracy over plus/minus...

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

Class I — Serious Health HazardOngoing
Medical DeviceJune 15, 2020· Luminex Corporation

Recalled Item: Verigene Processor SP with assay Luminex Recalled by Luminex Corporation Due...

The Issue: An instrument failure mode that may result in a Blood Culture Gram Positive...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 15, 2020· Luminex Corporation

Recalled Item: Verigene Processor SP with assay: Luminex Recalled by Luminex Corporation...

The Issue: An instrument failure mode that may result in a Blood Culture Gram Positive...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 15, 2020· Access Scientific LLC

Recalled Item: POWERWAND XL 4Fr 8cm Maximum Barrier Kit (Introducer with an Recalled by...

The Issue: Convenience kit mislabeled with the incorrect catheter effective length on...

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

Class III — Low RiskOngoing
DrugJune 13, 2020· Yusef Manufacturing Laboratories, LLC

Recalled Item: Tropical Lip Moisturizer Recalled by Yusef Manufacturing Laboratories, LLC...

The Issue: Superpotent Drug: The beginning portion of the batch appears to be...

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

Class II — Potential Health HazardOngoing
Refund
DrugJune 12, 2020· Beaming White Llc

Recalled Item: Koala Hand Sanitizer Recalled by Beaming White Llc Due to Undeclared Isopropyl

The Issue: Subpotent Drug: active ingredient ethanol tested below label claim and there...

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

Class II — Potential Health HazardOngoing
Refund
DrugJune 12, 2020· The Harvard Drug Group

Recalled Item: Metformin Hydrochloride Extended-Release Tablets Recalled by The Harvard...

The Issue: CGMP Deviation: Potential presence of Nitrosodimethylamine (NDMA) Impurity...

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

Class II — Potential Health HazardOngoing
Refund
DrugJune 12, 2020· Beaming White Llc

Recalled Item: Koala Hand Sanitizer Recalled by Beaming White Llc Due to Undeclared Isopropyl

The Issue: Subpotent Drug: active ingredient ethanol tested below label claim and there...

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

Class II — Potential Health HazardOngoing
Refund
DrugJune 12, 2020· Beaming White Llc

Recalled Item: Koala Hand Sanitizer Recalled by Beaming White Llc Due to Undeclared Isopropyl

The Issue: Subpotent Drug: active ingredient ethanol tested below label claim and there...

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

Class II — Potential Health HazardOngoing
Refund
DrugJune 12, 2020· Aurobindo Pharma USA Inc.

Recalled Item: Clozapine Tablets USP tablet Recalled by Aurobindo Pharma USA Inc. Due to...

The Issue: Presence of foreign tablet: Consumer complaint of Clozapine Tablets 50mg...

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

Class II — Potential Health HazardOngoing
Refund
FoodJune 12, 2020· NOW Health Group Inc.

Recalled Item: NOW Real Food Raw Macadamia Nuts Unsalted 8 oz retail Recalled by NOW Health...

The Issue: The product tested positive for Salmonella enterica.

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

Class I — Serious Health HazardOngoing
Refund
Medical DeviceJune 12, 2020· Medtronic Xomed, Inc.

Recalled Item: Software 1898072 IPC upgrade v 2.7.3.0 - Product Usage: The Recalled by...

The Issue: During internal testing execution of the next generation of Integrated Power...

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

Class II — Potential Health HazardOngoing
DrugJune 11, 2020· Hikma Pharmaceuticals USA Inc.

Recalled Item: Irinotecan HCL Injection Recalled by Hikma Pharmaceuticals USA Inc. Due to...

The Issue: Defective Container: Customer complaints received of a crimp defect while...

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

Class II — Potential Health HazardOngoing
Refund
DrugJune 11, 2020· Hikma Pharmaceuticals USA Inc.

Recalled Item: Irinotecan HCL Injection Recalled by Hikma Pharmaceuticals USA Inc. Due to...

The Issue: Defective Container: Customer complaints received of a crimp defect while...

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

Class II — Potential Health HazardOngoing
Refund
DrugJune 10, 2020· American Health Packaging

Recalled Item: Nabumetone Tablets Recalled by American Health Packaging Due to Labeling Not...

The Issue: Labeling Not Elsewhere Classified: The statement Pharmacist: Dispense with...

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

Class III — Low RiskOngoing
Refund
DrugJune 10, 2020· Crown Laboratories

Recalled Item: Nystatin Cream Recalled by Crown Laboratories Due to Subpotent Drug: Out of...

The Issue: Subpotent Drug: Out of specification for assay at the 9-month interval for...

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

Class II — Potential Health HazardOngoing
Refund