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 1012110140 of 46,762 recalls

Medical DeviceDecember 2, 2022· Covidien, LP

Recalled Item: Custom Suture Pack Product Description: US1638 CUSTOM SUTURE PACK US1756...

The Issue: Sterile Barrier Breach of Breather Pouch may cause infection or vision loss...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 2, 2022· Covidien, LP

Recalled Item: Ti-Cron Coated Braided Polyester Suture Product Description 88862775-31...

The Issue: Sterile Barrier Breach of Breather Pouch may cause infection or vision loss...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 2, 2022· Covidien, LP

Recalled Item: Surgidac Uncoated Braided Polyester suture Product Description D-1764K...

The Issue: Sterile Barrier Breach of Breather Pouch may cause infection or vision loss...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 2, 2022· Covidien, LP

Recalled Item: Sofsilk Coated Braided Silk Suture Product Description CS-211 SOFSILK* 4-0...

The Issue: Sterile Barrier Breach of Breather Pouch may cause infection or vision loss...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 2, 2022· Covidien, LP

Recalled Item: Monosof Monofilament Nylon sutures: Product Description CN-724 MONOSOF* 1...

The Issue: Sterile Barrier Breach of Breather Pouch may cause infection or vision loss...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 2, 2022· Covidien, LP

Recalled Item: Surgipro II Monofilament Polypropylene Sutures Product Description Model...

The Issue: Sterile Barrier Breach of Breather Pouch may cause infection or vision loss...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 2, 2022· Covidien, LP

Recalled Item: Monofilament Nylon Suture (McKesson Branded) and Coated Braided Silk Suture...

The Issue: Sterile Barrier Breach of Breather Pouch may cause infection or vision loss...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 2, 2022· Covidien, LP

Recalled Item: Novafil Monofilament Polybutester Suture Product Description: 8886 4002-41...

The Issue: Sterile Barrier Breach of Breather Pouch may cause infection or vision loss...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 2, 2022· Covidien, LP

Recalled Item: Surgipro Monofilament Polypropylene Sutures Product Description CP-535...

The Issue: Sterile Barrier Breach of Breather Pouch may cause infection or vision loss...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 2, 2022· Integra LifeSciences Corp.

Recalled Item: Codman Surgical Patties Recalled by Integra LifeSciences Corp. Due to...

The Issue: Integra LifeSciences identified that one lot was released with...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 2, 2022· Tomy International Inc.

Recalled Item: Lamaze Chill Teether Recalled by Tomy International Inc. Due to Affected...

The Issue: Affected lots of the product are being recalled due to potential microbial...

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

Class II — Potential Health HazardOngoing
DrugDecember 1, 2022· SUN PHARMACEUTICAL INDUSTRIES INC

Recalled Item: Oxcarbazepine Tablets 600mg Recalled by SUN PHARMACEUTICAL INDUSTRIES INC...

The Issue: Presence of foreign substance

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

Class II — Potential Health HazardOngoing
Refund
Medical DeviceNovember 30, 2022· Bayer Medical Care, Inc.

Recalled Item: Source Administration Set (SAS) used with the Medrad Intego PET Infusion...

The Issue: Black specks may be present on the packaged needles

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 30, 2022· Altimate Medical, Inc.

Recalled Item: ActiveAid 922 Recalled by Altimate Medical, Inc. Due to Device manufactured...

The Issue: Device manufactured with a component with affects the foldability of the...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 30, 2022· Beaver Visitec International, Inc.

Recalled Item: Beaver EdgeAhead Stiletto/MVR Knife .90mm Straight (20G)-for ocular...

The Issue: Packaging sterile barrier has been compromised. Open seals can lead to a...

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

Class II — Potential Health HazardOngoing
DrugNovember 29, 2022· Accord Healthcare, Inc.

Recalled Item: Daptomycin for Injection 350 mg/vial 1 Single-dose vial Recalled by Accord...

The Issue: Labeling mixup: cartons labeled as Daptomycin 350 mg/vial were found to...

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

Class I — Serious Health HazardOngoing
Refund
Medical DeviceNovember 29, 2022· Biomet, Inc.

Recalled Item: OSS Modular Arthrodesis Nail Recalled by Biomet, Inc. Due to Product missing...

The Issue: Product missing the four small locking collar bolts resulting in extension...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 29, 2022· Acumed LLC

Recalled Item: Acutrak 2 Part Number/Part Description: 30-0021 25.0mm Acutrak 2¿ - Recalled...

The Issue: Distribution without Pre-Market Clearance

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 29, 2022· Acumed LLC

Recalled Item: Dual-Trak Clavicle Screws Part Number/Part Description: 40-0136 3.0mm x 80mm...

The Issue: Distribution without Pre-Market Clearance

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 29, 2022· Acumed LLC

Recalled Item: AcuTwist Acutrak Compression Screws Part Number/Part Description: AI-0010-S...

The Issue: Distribution without Pre-Market Clearance

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

Class II — Potential Health HazardOngoing