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. 1,027 recalls have been distributed to Alaska in the last 12 months.

46,762 total recalls
1,027 in last 12 months

Showing 15921–15940 of 46,762 recalls

DrugDecember 17, 2020· CIPLA

Recalled Item: Esomeprazole Magnesium for Delayed-Release Oral Suspension 40mg Recalled by...

The Issue: Cross- contamination with other products: The excipient, Crospovidone, NF is...

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

Class II — Potential Health HazardOngoing
Refund
DrugDecember 17, 2020· CIPLA

Recalled Item: Esomeprazole Magnesium for Delayed-Release Oral Suspension 20mg Recalled by...

The Issue: Cross- contamination with other products: The excipient, Crospovidone, NF is...

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

Class II — Potential Health HazardOngoing
Refund
DrugDecember 17, 2020· Fresenius Kabi USA, LLC

Recalled Item: Ketorolac Tromethamine Injection Recalled by Fresenius Kabi USA, LLC Due to...

The Issue: Presence of Particulate Matter - found in reserve sample vials at the firm.

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

Class II — Potential Health HazardOngoing
Refund
DrugDecember 17, 2020· SCA Pharmaceuticals

Recalled Item: Lidocaine HCl 2% 5 mL Recalled by SCA Pharmaceuticals Due to Lack of...

The Issue: Lack of Assurance of Sterility; potential for a defective syringe cap,...

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

Class II — Potential Health HazardOngoing
Refund
DrugDecember 17, 2020· Ascend Laboratories LLC

Recalled Item: Ascend Laboratories Recalled by Ascend Laboratories LLC Due to Failed...

The Issue: Failed Impurity/Degradation Specifications

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

Class II — Potential Health HazardOngoing
Refund
DrugDecember 17, 2020· Ascend Laboratories LLC

Recalled Item: Ascend Laboratories Recalled by Ascend Laboratories LLC Due to Failed...

The Issue: Failed Impurity/Degradation Specifications

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

Class II — Potential Health HazardOngoing
Refund
DrugDecember 17, 2020· SCA Pharmaceuticals

Recalled Item: SUCcinylcholine Chloride 100 mg/5mL Recalled by SCA Pharmaceuticals Due to...

The Issue: Lack of Assurance of Sterility; potential for a defective syringe cap,...

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

Class II — Potential Health HazardOngoing
Refund
DrugDecember 17, 2020· CIPLA

Recalled Item: Esomeprazole Magnesium for Delayed-Release Oral Suspension 10mg Recalled by...

The Issue: Cross- contamination with other products: The excipient, Crospovidone, NF is...

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

Class II — Potential Health HazardOngoing
Refund
DrugDecember 17, 2020· NDAL Mfg Inc.

Recalled Item: ManukaGuard Medical Grade Manuka Honey Allercleanse Nasal Spray Recalled by...

The Issue: Microbial Contamination of Non-Sterile Products: Product confirmed to have yeast

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

Class I — Serious Health HazardOngoing
Refund
DrugDecember 17, 2020· SCA Pharmaceuticals

Recalled Item: Ketamine 100 mg/10mL in 0.9% Sodium Chloride Injection (10 mg/mL) Recalled...

The Issue: Lack of Assurance of Sterility; potential for a defective syringe cap,...

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

Class II — Potential Health HazardOngoing
Refund
DrugDecember 16, 2020· US Compounding Inc

Recalled Item: Succinylcholine Chloride PF Inj. 200 mg/10 mL Recalled by US Compounding Inc...

The Issue: Labeling: Incorrect or Missing lot and/or expiration date: The lot number...

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

Class III — Low RiskOngoing
Refund
Medical DeviceDecember 16, 2020· Medtronic Neurosurgery

Recalled Item: X1 Recalled by Medtronic Neurosurgery Due to Neonatal Valves were...

The Issue: Neonatal Valves were manufactured with a ventricular catheter connection...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 16, 2020· Microbiologics Inc

Recalled Item: KWIK-STI(TM) Recalled by Microbiologics Inc Due to The expiration date on...

The Issue: The expiration date on the label of one component (negative control 0243U)...

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

Class III — Low RiskOngoing
Medical DeviceDecember 16, 2020· Cook Medical Llc

Recalled Item: Disposable Humidification Flask Recalled by Cook Medical Llc Due to A small...

The Issue: A small percentage of the Disposable Humidification Flasks may have a...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 16, 2020· Medtronic Neurosurgery

Recalled Item: X1 Recalled by Medtronic Neurosurgery Due to Neonatal Valves were...

The Issue: Neonatal Valves were manufactured with a ventricular catheter connection...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 16, 2020· Medtronic Neurosurgery

Recalled Item: X1 Recalled by Medtronic Neurosurgery Due to Neonatal Valves were...

The Issue: Neonatal Valves were manufactured with a ventricular catheter connection...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 15, 2020· Penumbra Inc.

Recalled Item: Penumbra JET 7MAX KIT Penumbra JET 7 Reperfusion Catheter+ MAX Recalled by...

The Issue: The catheter may become susceptible to distal tip damage during use. Distal...

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

Class I — Serious Health HazardOngoing
Medical DeviceDecember 15, 2020· Boston Scientific Corporation

Recalled Item: ACUITY Universal Cutter Recalled by Boston Scientific Corporation Due to...

The Issue: Boston Scientific (BSC) is retrieving five Model 7060 ACUITY cutters...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 15, 2020· Penumbra Inc.

Recalled Item: Penumbra JET 7 KIT Reperfusion Catheter+Penumbra Hi-Flow Aspiration Tubing...

The Issue: The catheter may become susceptible to distal tip damage during use. Distal...

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

Class I — Serious Health HazardOngoing
Medical DeviceDecember 15, 2020· Ortho Clinical Diagnostics Inc

Recalled Item: VITROS XT Chemistry Products ALB-TP Slides (ALB is not affected) Recalled by...

The Issue: Eltrombopag Interference for VITROS Chemistry Products TP Slides and VITROS...

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

Class II — Potential Health HazardOngoing