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. 2,336 recalls have been distributed to Alaska in the last 12 months.

46,762 total recalls
2,336 in last 12 months

Showing 2856128580 of 46,762 recalls

DrugApril 18, 2017· Key Pharmacy and Compounding Center

Recalled Item: ATROPINE SULFATE 0.01% OPHTH Recalled by Key Pharmacy and Compounding Center...

The Issue: Lack of Assurance of Sterility: The firm is recalling sterile compounded...

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

Class II — Potential Health HazardOngoing
Refund
DrugApril 18, 2017· Key Pharmacy and Compounding Center

Recalled Item: PYRIDOXAL-5-PHOS 5ML MDV 50MG/ML INJ Recalled by Key Pharmacy and...

The Issue: Lack of Assurance of Sterility: The firm is recalling sterile compounded...

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

Class II — Potential Health HazardOngoing
Refund
DrugApril 18, 2017· Key Pharmacy and Compounding Center

Recalled Item: VITAMIN B COMPLEX 1ML SDV NA INJ Recalled by Key Pharmacy and Compounding...

The Issue: Lack of Assurance of Sterility: The firm is recalling sterile compounded...

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

Class II — Potential Health HazardOngoing
Refund
DrugApril 18, 2017· Key Pharmacy and Compounding Center

Recalled Item: TRI MIX 20/30/1 5ML MDV MCG/MG/MG/ML INJ Recalled by Key Pharmacy and...

The Issue: Lack of Assurance of Sterility: The firm is recalling sterile compounded...

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

Class II — Potential Health HazardOngoing
Refund
DrugApril 18, 2017· Key Pharmacy and Compounding Center

Recalled Item: TRI MIX 5/30/0.5 5ML MDV MCG/MG/MG/ML INJ Recalled by Key Pharmacy and...

The Issue: Lack of Assurance of Sterility: The firm is recalling sterile compounded...

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

Class II — Potential Health HazardOngoing
Refund
DrugApril 18, 2017· Key Pharmacy and Compounding Center

Recalled Item: PROGESTERONE SESAME OIL 10ML MDV 100MG/ML INJ Recalled by Key Pharmacy and...

The Issue: Lack of Assurance of Sterility: The firm is recalling sterile compounded...

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

Class II — Potential Health HazardOngoing
Refund
DrugApril 18, 2017· Key Pharmacy and Compounding Center

Recalled Item: FERR GLUC MDV 60MG/ML INJ Recalled by Key Pharmacy and Compounding Center...

The Issue: Lack of Assurance of Sterility: The firm is recalling sterile compounded...

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

Class II — Potential Health HazardOngoing
Refund
DrugApril 18, 2017· Key Pharmacy and Compounding Center

Recalled Item: DMSO 6.25% OPHTH. Recalled by Key Pharmacy and Compounding Center Due to...

The Issue: Lack of Assurance of Sterility: The firm is recalling sterile compounded...

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

Class II — Potential Health HazardOngoing
Refund
DrugApril 17, 2017· P & L Development, LLC

Recalled Item: Allergy Relief Diphenhydramine HCl 25 mg Recalled by P & L Development, LLC...

The Issue: Subpotent: This product is being recalled due to low out of specification...

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

Class III — Low RiskOngoing
Refund
DrugApril 17, 2017· Fagron, Inc

Recalled Item: Zinc Oxide Paste 25% Recalled by Fagron, Inc Due to Labeling: Error on...

The Issue: Labeling: Error on Declared Strength: Error is due to an incorrect value in...

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

Class III — Low RiskOngoing
Refund
Medical DeviceApril 17, 2017· Zimmer Biomet, Inc.

Recalled Item: AFFIXUS Hip Fracture Nail Product Usage: The Hip Fracture Nail Recalled by...

The Issue: nail not properly engaging with the targeting jig due to certain undersized...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 14, 2017· Cardiovascular Systems Inc

Recalled Item: CSI Recalled by Cardiovascular Systems Inc Due to Cardiovascular Systems,...

The Issue: Cardiovascular Systems, Inc. (CSI). has initiated a recall to remove 1,396...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 13, 2017· Pentax of America Inc

Recalled Item: 9400 Laryngeal Strobe Product Usage: The 9310HD is used to Recalled by...

The Issue: Pentax Medical did not always provide transformers with 9175 isolation...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 13, 2017· Pentax of America Inc

Recalled Item: 9310HD Digital Video Capture Modules Product Usage: The 9310HD is Recalled...

The Issue: Pentax Medical did not always provide transformers with 9175 isolation...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 13, 2017· Pentax of America Inc

Recalled Item: 7245C Recalled by Pentax of America Inc Due to Pentax Medical did not always...

The Issue: Pentax Medical did not always provide transformers with 9175 isolation...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 13, 2017· BioMerieux SA

Recalled Item: ETEST OXACILLIN OX 256 WW F100 In vitro diagnostic Recalled by BioMerieux SA...

The Issue: QC failures (MIC out of range high) for S.aureus ATCC 29213 strain on ETEST...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 13, 2017· BioMerieux SA

Recalled Item: ETEST OXACILLIN OX 256 US F100 In vitro diagnostic Recalled by BioMerieux SA...

The Issue: QC failures (MIC out of range high) for S.aureus ATCC 29213 strain on ETEST...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 13, 2017· CardioTek BV

Recalled Item: CardioTek EP-TRACER Software V1.x and V2.0 The EP-TRACER System is Recalled...

The Issue: Software bug which allows parameters to be changed unintentionally during use.

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 13, 2017· Pentax of America Inc

Recalled Item: 9200C and 9200D Laryngeal Strobe Product Usage: The 9310HD is Recalled by...

The Issue: Pentax Medical did not always provide transformers with 9175 isolation...

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

Class II — Potential Health HazardOngoing
DrugApril 13, 2017· Standard Homeopathic Company

Recalled Item: Hyland's Baby Nighttime Teething Tablets [Belladonna 12X HPUS...

The Issue: Superpotent Drug: FDA analysis found inconsistent amounts of belladonna...

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

Class I — Serious Health HazardOngoing
Refund