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. 2,480 recalls have been distributed to Alaska in the last 12 months.

46,762 total recalls
2,480 in last 12 months

Showing 1408114100 of 46,762 recalls

Medical DeviceAugust 9, 2021· Ad-Tech Medical Instrument Corporation

Recalled Item: Ad-Tech Lightweight TECH ATTACH Cable - Product Usage: Designed for Recalled...

The Issue: Incorrect version of labels were used.

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 9, 2021· Ad-Tech Medical Instrument Corporation

Recalled Item: Ad-Tech Lightweight CABRIO Cable - Product Usage: Designed for the Recalled...

The Issue: Incorrect version of labels were used.

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 9, 2021· Ad-Tech Medical Instrument Corporation

Recalled Item: Ad-Tech TECH ATTACH Cable- Product Usage: Designed for the purpose Recalled...

The Issue: Incorrect version of labels were used.

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

Class II — Potential Health HazardOngoing
DrugAugust 6, 2021· XELLIA PHARMACEUTICALS USA, LLC

Recalled Item: Micafungin for Injection Recalled by XELLIA PHARMACEUTICALS USA, LLC Due to...

The Issue: Labeling; Incorrect or Missing Package Insert: The package insert provided...

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

Class II — Potential Health HazardOngoing
Refund
DrugAugust 6, 2021· XELLIA PHARMACEUTICALS USA, LLC

Recalled Item: Micafungin for Injection Recalled by XELLIA PHARMACEUTICALS USA, LLC Due to...

The Issue: Labeling; Incorrect or Missing Package Insert: The package insert provided...

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

Class II — Potential Health HazardOngoing
Refund
Medical DeviceAugust 6, 2021· ZOLL Circulation, Inc.

Recalled Item: Zoll Recalled by ZOLL Circulation, Inc. Due to Labeling update concerning...

The Issue: Labeling update concerning potential leaks from the catheter or the start-up...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 6, 2021· ZOLL Circulation, Inc.

Recalled Item: ZOLL Recalled by ZOLL Circulation, Inc. Due to Labeling update concerning...

The Issue: Labeling update concerning potential leaks from the catheter or the start-up...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 6, 2021· ZOLL Circulation, Inc.

Recalled Item: ZOLL Recalled by ZOLL Circulation, Inc. Due to Labeling update concerning...

The Issue: Labeling update concerning potential leaks from the catheter or the start-up...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 6, 2021· ZOLL Circulation, Inc.

Recalled Item: Zoll Recalled by ZOLL Circulation, Inc. Due to Labeling update concerning...

The Issue: Labeling update concerning potential leaks from the catheter or the start-up...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 6, 2021· ZOLL Circulation, Inc.

Recalled Item: Zoll Recalled by ZOLL Circulation, Inc. Due to Labeling update concerning...

The Issue: Labeling update concerning potential leaks from the catheter or the start-up...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 6, 2021· Johnson & Johnson Surgical Vision Inc

Recalled Item: TECNIS Eyhance IOLs are permanent intraocular implants intended for...

The Issue: Nonconforming product was distributed in error. Product was nonconforming...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 6, 2021· ZOLL Circulation, Inc.

Recalled Item: Zoll (SL-2593CO) Recalled by ZOLL Circulation, Inc. Due to Labeling update...

The Issue: Labeling update concerning potential leaks from the catheter or the start-up...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 6, 2021· ZOLL Circulation, Inc.

Recalled Item: ZOLL Recalled by ZOLL Circulation, Inc. Due to Labeling update concerning...

The Issue: Labeling update concerning potential leaks from the catheter or the start-up...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 6, 2021· ZOLL Circulation, Inc.

Recalled Item: Zoll Recalled by ZOLL Circulation, Inc. Due to Labeling update concerning...

The Issue: Labeling update concerning potential leaks from the catheter or the start-up...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 6, 2021· ZOLL Circulation, Inc.

Recalled Item: Zoll Recalled by ZOLL Circulation, Inc. Due to Labeling update concerning...

The Issue: Labeling update concerning potential leaks from the catheter or the start-up...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 6, 2021· ZOLL Circulation, Inc.

Recalled Item: Zoll Recalled by ZOLL Circulation, Inc. Due to Labeling update concerning...

The Issue: Labeling update concerning potential leaks from the catheter or the start-up...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 6, 2021· ZOLL Circulation, Inc.

Recalled Item: Zoll (IC-3893CO) Recalled by ZOLL Circulation, Inc. Due to Labeling update...

The Issue: Labeling update concerning potential leaks from the catheter or the start-up...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 6, 2021· ZOLL Circulation, Inc.

Recalled Item: Zoll Recalled by ZOLL Circulation, Inc. Due to Labeling update concerning...

The Issue: Labeling update concerning potential leaks from the catheter or the start-up...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 6, 2021· ZOLL Circulation, Inc.

Recalled Item: Zoll Recalled by ZOLL Circulation, Inc. Due to Labeling update concerning...

The Issue: Labeling update concerning potential leaks from the catheter or the start-up...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 6, 2021· ZOLL Circulation, Inc.

Recalled Item: Zoll Recalled by ZOLL Circulation, Inc. Due to Labeling update concerning...

The Issue: Labeling update concerning potential leaks from the catheter or the start-up...

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

Class II — Potential Health HazardOngoing