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. 2,487 recalls have been distributed to Alaska in the last 12 months.

46,762 total recalls
2,487 in last 12 months

Showing 1348113500 of 46,762 recalls

Medical DeviceNovember 1, 2021· Smith & Nephew, Inc.

Recalled Item: smith&nephew EVOS MEDIAL DISTAL FEMUR PLATE Recalled by Smith & Nephew, Inc....

The Issue: Testing vendor notified Smith & Nephew that previous MRI scanning conditions...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 1, 2021· Randox Laboratories Ltd.

Recalled Item: RANDOX CHOL-cholesterol (total) test system intended to measure cholesterol...

The Issue: When calibrating using the standard provided in the kit, the change in...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 29, 2021· Diversatek Healthcare

Recalled Item: Diversatek Health Recalled by Diversatek Healthcare Due to M-Catch Retrieval...

The Issue: M-Catch Retrieval Nets, Part Number 1175-01 / Lot Number 001919, that were...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 29, 2021· Philips North America Llc

Recalled Item: Wireless Footswtich used with the following Philips Allura Xper and Recalled...

The Issue: Wireless foot switch connection issues causing interruption of Fluoroscopy...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 29, 2021· NuVasive Specialized Orthopedics, Inc.

Recalled Item: NUVASIVE PRECICE Intramedullary Limb Lengthening (IMLL) and (Short) System:...

The Issue: The Instructions for Use have been updated to include: (1) Clarification...

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

Class II — Potential Health HazardOngoing
DrugOctober 28, 2021· Teva Pharmaceuticals USA

Recalled Item: Clonidine Transdermal System Recalled by Teva Pharmaceuticals USA Due to...

The Issue: Failed Impurities/Degradation Specifications

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

Class III — Low RiskOngoing
Refund
FoodOctober 28, 2021· MARY RUTH ORGANICS

Recalled Item: MaryRuth's Organic Infants Liquid Probiotic Recalled by MARY RUTH ORGANICS...

The Issue: Internal testing found the presence of Pseudomonas aeruginosa in the product.

Recommended Action: Do not consume. Return to store for a refund or discard.

Class I — Serious Health HazardOngoing
Refund
Medical DeviceOctober 28, 2021· Palodex Group Oy

Recalled Item: Orthopantomograph OP300 dental computed tomography x-ray system. The X-ray...

The Issue: It was noticed in production on 28.10.2021, that the final testing database...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 28, 2021· Osteomed, LLC

Recalled Item: OsteoMed OsteoPower Power Console: -OsteoMed OsteoPower Power Console 2 by...

The Issue: Due to consoles not in compliance with the latest electrical safety...

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

Class II — Potential Health HazardOngoing
DrugOctober 27, 2021· Teva Pharmaceuticals USA

Recalled Item: Cartia XT (Diltiazem Hydrochloride Extended-Release Capsules Recalled by...

The Issue: Labelling: Incorrect Exp. Date

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

Class II — Potential Health HazardOngoing
Refund
Medical DeviceOctober 27, 2021· Medline Industries Inc

Recalled Item: EVLP Convenience Pack/Kit Recalled by Medline Industries Inc Due to NaCl 250...

The Issue: NaCl 250 mL Bag Inj expired 04/2020 while the kit expiration date was after...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 27, 2021· Medline Industries Inc

Recalled Item: Venous Access Pack-LF Convenience Kit Recalled by Medline Industries Inc Due...

The Issue: NaCl 250 mL Bag Inj expired 04/2020 while the kit expiration date was after...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 27, 2021· Medline Industries Inc

Recalled Item: Major Vascular CDS Convenience Kit Recalled by Medline Industries Inc Due to...

The Issue: NaCl 250 mL Bag Inj expired 04/2020 while the kit expiration date was after...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 27, 2021· Medline Industries Inc

Recalled Item: Bedside PICC CDS Convenience Kit Recalled by Medline Industries Inc Due to...

The Issue: NaCl 250 mL Bag Inj expired 04/2020 while the kit expiration date was after...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 27, 2021· Medline Industries Inc

Recalled Item: Neuro Convenience Kit Recalled by Medline Industries Inc Due to NaCl 250 mL...

The Issue: NaCl 250 mL Bag Inj expired 04/2020 while the kit expiration date was after...

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

Class II — Potential Health HazardOngoing
DrugOctober 26, 2021· VIRGIN SCENT INC

Recalled Item: artnaturals hand sanitizer Recalled by VIRGIN SCENT INC Due to CGMP...

The Issue: CGMP Deviations: Other lots recalled because they were manufactured using...

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

Class II — Potential Health HazardOngoing
Refund
DrugOctober 26, 2021· VIRGIN SCENT INC

Recalled Item: artnaturals Hand Sanitizer Recalled by VIRGIN SCENT INC Due to CGMP...

The Issue: CGMP Deviations: Other lots recalled because they were manufactured using...

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

Class II — Potential Health HazardOngoing
Refund
DrugOctober 26, 2021· VIRGIN SCENT INC

Recalled Item: artnaturals hand sanitizer Recalled by VIRGIN SCENT INC Due to Chemical...

The Issue: Chemical Contamination: presence of benzene, acetaldehyde, and acetal.

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

Class I — Serious Health HazardOngoing
Refund
DrugOctober 26, 2021· Perrigo Company PLC

Recalled Item: No Drip Nasal Spray Recalled by Perrigo Company PLC Due to CGMP Deviations:...

The Issue: CGMP Deviations: Products were manufactured with contaminated excipient that...

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

Class II — Potential Health HazardOngoing
Refund
DrugOctober 26, 2021· Perrigo Company PLC

Recalled Item: Acetaminophen Child Bubble Gum Flavored Oral Suspension (160 mg/5 ml)...

The Issue: CGMP Deviations: Products were manufactured with contaminated excipient that...

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

Class II — Potential Health HazardOngoing
Refund