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. 2,534 recalls have been distributed to Alaska in the last 12 months.

46,762 total recalls
2,534 in last 12 months

Showing 37213740 of 46,762 recalls

DrugNovember 6, 2024· Trinity Gold Nutrition

Recalled Item: Trinity Gold Nutrition Recalled by Trinity Gold Nutrition Due to Undeclared...

The Issue: Marketed without an Approved NDA/ANDA: FDA analysis found product to be...

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

Class II — Potential Health HazardOngoing
Refund
Medical DeviceNovember 6, 2024· MEDLINE INDUSTRIES, LP - Northfield

Recalled Item: Medline brand Recalled by MEDLINE INDUSTRIES, LP - Northfield Due to...

The Issue: Surgical Patties & Surgical Strips in specific lots of Custom Convenience...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 6, 2024· MEDLINE INDUSTRIES, LP - Northfield

Recalled Item: KIT Recalled by MEDLINE INDUSTRIES, LP - Northfield Due to Surgical Patties...

The Issue: Surgical Patties & Surgical Strips in specific lots of Custom Convenience...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 6, 2024· MEDLINE INDUSTRIES, LP - Northfield

Recalled Item: SEPTOPLASTY PACK Convenient kit Recalled by MEDLINE INDUSTRIES, LP -...

The Issue: Surgical Patties & Surgical Strips in specific lots of Custom Convenience...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 6, 2024· MEDLINE INDUSTRIES, LP - Northfield

Recalled Item: Medline brand Recalled by MEDLINE INDUSTRIES, LP - Northfield Due to...

The Issue: Surgical Patties & Surgical Strips in specific lots of Custom Convenience...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 6, 2024· MEDLINE INDUSTRIES, LP - Northfield

Recalled Item: DIEP FLAP Convenience kit Recalled by MEDLINE INDUSTRIES, LP - Northfield...

The Issue: Surgical Patties & Surgical Strips in specific lots of Custom Convenience...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 6, 2024· MEDLINE INDUSTRIES, LP - Northfield

Recalled Item: FESS-MB PACK-LF Convenience kit Recalled by MEDLINE INDUSTRIES, LP -...

The Issue: Surgical Patties & Surgical Strips in specific lots of Custom Convenience...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 6, 2024· MEDLINE INDUSTRIES, LP - Northfield

Recalled Item: Medline brand Recalled by MEDLINE INDUSTRIES, LP - Northfield Due to...

The Issue: Surgical Patties & Surgical Strips in specific lots of Custom Convenience...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 6, 2024· MEDLINE INDUSTRIES, LP - Northfield

Recalled Item: Medline brand Recalled by MEDLINE INDUSTRIES, LP - Northfield Due to...

The Issue: Surgical Patties & Surgical Strips in specific lots of Custom Convenience...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 6, 2024· MEDLINE INDUSTRIES, LP - Northfield

Recalled Item: MAJOR NEURO PACK-LF Convenience kit Recalled by MEDLINE INDUSTRIES, LP -...

The Issue: Surgical Patties & Surgical Strips in specific lots of Custom Convenience...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 6, 2024· MEDLINE INDUSTRIES, LP - Northfield

Recalled Item: Medline brand Recalled by MEDLINE INDUSTRIES, LP - Northfield Due to...

The Issue: Surgical Patties & Surgical Strips in specific lots of Custom Convenience...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 6, 2024· ICU Medical, Inc.

Recalled Item: ChemoLock Close Vial Spike The Chemolock Closed System Recalled by ICU...

The Issue: Due to finished goods incorrectly packaged and labeled.

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 6, 2024· Becton Dickinson & Co.

Recalled Item: BD BBL Sensi Disc Ampicillin 2 ¿g (AM-2) - In-Vitro Recalled by Becton...

The Issue: BD identified through potency testing as part of a stability test request to...

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

Class II — Potential Health HazardOngoing
DrugNovember 5, 2024· The Harvard Drug Group LLC dba Major Pharmaceuticals and Rugby Laboratories

Recalled Item: Hydralazine HCl Tablets Recalled by The Harvard Drug Group LLC dba Major...

The Issue: Failed Impurities/Degradation Specifications; during routine stability...

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

Class III — Low RiskOngoing
Refund
Medical DeviceNovember 5, 2024· Microline Surgical, Inc.

Recalled Item: Microscissor Tip (Disposable) Recalled by Microline Surgical, Inc. Due to A...

The Issue: A lot of ReNew Microscissor Tips exhibited a 2% rate of failure in terms of...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 5, 2024· KCI USA, INC.

Recalled Item: V.A.C. Ulta Therapy Unit & ULTDEV01 The 3M" Recalled by KCI USA, INC. Due to...

The Issue: Due to potential system error alarm and the inability to initiate therapy as...

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

Class II — Potential Health HazardOngoing
DrugNovember 4, 2024· Boulla LLC

Recalled Item: ZapMax Capsules Recalled by Boulla LLC Due to Undeclared Sildenafil

The Issue: Marketed without an approved NDA/ANDA: Products found to contain undeclared...

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

Class I — Serious Health HazardOngoing
Refund
DrugNovember 4, 2024· Boulla LLC

Recalled Item: VitalityXtra Capsules Recalled by Boulla LLC Due to Undeclared Sildenafil

The Issue: Marketed without an approved NDA/ANDA: Products found to contain undeclared...

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

Class I — Serious Health HazardOngoing
Refund
DrugNovember 4, 2024· Boulla LLC

Recalled Item: PeakMax Capsules Recalled by Boulla LLC Due to Undeclared Sildenafil

The Issue: Marketed without an approved NDA/ANDA: Products found to contain undeclared...

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

Class I — Serious Health HazardOngoing
Refund
DrugNovember 4, 2024· Boulla LLC

Recalled Item: ZoomMax Capsules Recalled by Boulla LLC Due to Undeclared Sildenafil

The Issue: Marketed without an approved NDA/ANDA: Products found to contain undeclared...

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

Class I — Serious Health HazardOngoing
Refund