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. 2,508 recalls have been distributed to Alaska in the last 12 months.

46,762 total recalls
2,508 in last 12 months

Showing 1008110100 of 46,762 recalls

Medical DeviceDecember 7, 2022· The Anspach Effort, Inc.

Recalled Item: Pediatric Craniotome Recalled by The Anspach Effort, Inc. Due to Ball...

The Issue: Ball bearings in the CRANI-A (ANSPACH Power Tools Adult Craniotome...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 7, 2022· The Anspach Effort, Inc.

Recalled Item: Adult Craniotome Recalled by The Anspach Effort, Inc. Due to Ball bearings...

The Issue: Ball bearings in the CRANI-A (ANSPACH Power Tools Adult Craniotome...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 7, 2022· Siemens Healthcare Diagnostics, Inc.

Recalled Item: IMMULITE 2000 Thyroglobulin (US)- For in vitro diagnostic use with Recalled...

The Issue: Potential for Functional Sensitivity to not meet Instructions For Use (IFU)...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 7, 2022· The Anspach Effort, Inc.

Recalled Item: 7.5 cm Large Rotating Craniotome Attachment. Use with XMax¿ Recalled by The...

The Issue: Ball bearings in the CRANI-A (ANSPACH Power Tools Adult Craniotome...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 7, 2022· Covidien LP

Recalled Item: MAHURKAR 13.5Fr High Flow Dual Lumen Acute Dialysis Catheter Recalled by...

The Issue: There is a potential leaking condition within the hub of affected devices,...

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

Class I — Serious Health HazardOngoing
Medical DeviceDecember 7, 2022· The Anspach Effort, Inc.

Recalled Item: 6.5 cm Pediatric Craniotome Attachment. Use with XMax¿ Recalled by The...

The Issue: Ball bearings in the CRANI-A (ANSPACH Power Tools Adult Craniotome...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 7, 2022· The Anspach Effort, Inc.

Recalled Item: 7.5 cm Large Craniotome Attachment Use with XMax¿ Recalled by The Anspach...

The Issue: Ball bearings in the CRANI-A (ANSPACH Power Tools Adult Craniotome...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 7, 2022· Philips Respironics, Inc.

Recalled Item: Philips Trilogy 200 Ventilator Recalled by Philips Respironics, Inc. Due to...

The Issue: The replacement silicone sound abatement foam installed into some Trilogy...

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

Class I — Serious Health HazardOngoing
Medical DeviceDecember 7, 2022· The Anspach Effort, Inc.

Recalled Item: 6.5 cm Adult Rotating Craniotome Attachment. Use with XMax¿ Recalled by The...

The Issue: Ball bearings in the CRANI-A (ANSPACH Power Tools Adult Craniotome...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 7, 2022· The Anspach Effort, Inc.

Recalled Item: 6.5 cm Adult Craniotome Recalled by The Anspach Effort, Inc. Due to Ball...

The Issue: Ball bearings in the CRANI-A (ANSPACH Power Tools Adult Craniotome...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 7, 2022· The Anspach Effort, Inc.

Recalled Item: 6.5 cm Adult Rotating Craniotome Attachment. Use with XMax¿ Recalled by The...

The Issue: Ball bearings in the CRANI-A (ANSPACH Power Tools Adult Craniotome...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 7, 2022· The Anspach Effort, Inc.

Recalled Item: Adult Craniotome Intended for cutting and shaping bone Recalled by The...

The Issue: Ball bearings in the CRANI-A (ANSPACH Power Tools Adult Craniotome...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 7, 2022· Siemens Healthcare Diagnostics, Inc.

Recalled Item: IMMULITE 2000 Thyroglobulin (OUS). For in vitro diagnostic use with Recalled...

The Issue: Potential for Functional Sensitivity to not meet Instructions For Use (IFU)...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 7, 2022· Philips Respironics, Inc.

Recalled Item: Philips Garbin Ventilator Recalled by Philips Respironics, Inc. Due to The...

The Issue: The replacement silicone sound abatement foam installed into some Trilogy...

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

Class I — Serious Health HazardOngoing
DrugDecember 6, 2022· Glaxosmithkline Consumer Healthcare Holdings DBA Haleon

Recalled Item: Advil Liqui Gels (minis) Recalled by Glaxosmithkline Consumer Healthcare...

The Issue: Labeling: Illegible Label; the adhesive migrated onto a portion of the...

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

Class I — Serious Health HazardOngoing
Refund
DrugDecember 6, 2022· Glaxosmithkline Consumer Healthcare Holdings DBA Haleon

Recalled Item: Advil Liqui Gels Recalled by Glaxosmithkline Consumer Healthcare Holdings...

The Issue: Labeling: Illegible Label; the adhesive migrated onto a portion of the...

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

Class I — Serious Health HazardOngoing
Refund
DrugDecember 6, 2022· Glaxosmithkline Consumer Healthcare Holdings DBA Haleon

Recalled Item: Advil (ibuprofen) Tablets Recalled by Glaxosmithkline Consumer Healthcare...

The Issue: Labeling: Illegible Label; the adhesive migrated onto a portion of the...

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

Class I — Serious Health HazardOngoing
Refund
DrugDecember 6, 2022· Camber Pharmaceuticals, Inc

Recalled Item: Lacosamide Oral Solution Recalled by Camber Pharmaceuticals, Inc Due to...

The Issue: Failed Excipient Specifications: out of specification result observed for...

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

Class III — Low RiskOngoing
Refund
Medical DeviceDecember 6, 2022· Zimmer, Inc.

Recalled Item: NexGen Option Stemmed Tibial Component Size 7 Recalled by Zimmer, Inc. Due...

The Issue: Zimmer Biomet is conducting a voluntary medical device recall related to the...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 6, 2022· Zimmer, Inc.

Recalled Item: NexGen Option Stemmed Tibial Component Size 5 Recalled by Zimmer, Inc. Due...

The Issue: Zimmer Biomet is conducting a voluntary medical device recall related to the...

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

Class II — Potential Health HazardOngoing