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. 2,503 recalls have been distributed to Alaska in the last 12 months.

46,762 total recalls
2,503 in last 12 months

Showing 1068110700 of 27,254 recalls

Medical DeviceOctober 8, 2020· Canon Medical System, USA, INC.

Recalled Item: CAS-930A Flat Panel Monitor (FPD) used in conjunction with the Recalled by...

The Issue: There is a potential that the cable of the Flat panel detector may break...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 8, 2020· RAYSEARCH LABORATORIES AB

Recalled Item: RayStation standalone software treatment planning system Recalled by...

The Issue: If a region of interest (ROI) or point of interest (POI) that is from an...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 8, 2020· Microbiologics Inc

Recalled Item: Catalog 02145P Recalled by Microbiologics Inc Due to Strain should be VIM-1...

The Issue: Strain should be VIM-1 positive but is confirmed to be VIM-1 negative.

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 7, 2020· Steris Corporation

Recalled Item: Olympus Leak Test Adapter used with Acu-sInQ Complete Endoscope Cleaning...

The Issue: Potential for cleaning solution intrusion into endoscope

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

Class III — Low RiskOngoing
Medical DeviceOctober 6, 2020· Arjohuntleigh Magog, Inc.

Recalled Item: Arjo Flat Dynamic Positioning System (DPS) - Product Usage: used Recalled by...

The Issue: Risk of Sling Clip breakage while in use with obsolete Flat Dynamic...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 6, 2020· Hardy Diagnostics

Recalled Item: Strep B Carrot Broth One-Step Recalled by Hardy Diagnostics Due to...

The Issue: Streptococcus culture medium contains an incorrect expiration date. The...

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

Class III — Low RiskOngoing
Medical DeviceOctober 5, 2020· Thera Test Laboratories, Inc.

Recalled Item: EL-Anti-SARS-CoV-2 IgG Kit Recalled by Thera Test Laboratories, Inc. Due to...

The Issue: The cross-reactivity of the device may present an increased level of...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 5, 2020· Becton, Dickinson and Company, BD Biosciences

Recalled Item: BD" Multi-Check CD4 Low Control 2.5 mL IVD - Product Recalled by Becton,...

The Issue: Recent product complaints showing an unexpected cell population exhibiting...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 5, 2020· Bayer Medical Care, Inc.

Recalled Item: Brand Name: MEDRAD Stellant FLEX Syringe Kits Common Name: Angiographic...

The Issue: Specific lots of MEDRAD Stellant FLEX 150 mL syringe kits may have holes...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 5, 2020· Micro-Tech Usa

Recalled Item: Elastic Traction Device Recalled by Micro-Tech Usa Due to FDA has informed...

The Issue: FDA has informed Micro-Tech that the Elastic Traction Device is not...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 1, 2020· Microbiologics Inc

Recalled Item: KWIK-STIK(TM) Recalled by Microbiologics Inc Due to Potential E. coli...

The Issue: Potential contamination with S. epidermidis E. coli and S. warneri.

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 1, 2020· Microbiologics Inc

Recalled Item: QC Sets and Panels: KWIK-STIK" 2 Pack. Common Name: QC Recalled by...

The Issue: Potential contamination with Escherichia coli Staphylococcus epidermidis and...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 1, 2020· Microbiologics Inc

Recalled Item: LYFO DISK(TM) Recalled by Microbiologics Inc Due to Potential E. coli...

The Issue: Potential contamination with Escherichia coli, Staphylococcus epidermidis...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 1, 2020· Bard Peripheral Vascular Inc

Recalled Item: Bard Conquest PTA Balloon dilation Catheter Recalled by Bard Peripheral...

The Issue: Dilation catheter packaged with the wrong size balloon. The labeling states...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 30, 2020· Ortho Clinical Diagnostics Inc

Recalled Item: VITROS¿ Immunodiagnostic Products Anti-SARS-CoV-2 IgG Control - Product...

The Issue: Elevated sample results signal/cutoff (s/c) values when using eight (8) lots...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 30, 2020· Ortho Clinical Diagnostics Inc

Recalled Item: VITROS Immunodiagnostic Products-SARS-CoV-2 IgG Calibrator - Product Usage:...

The Issue: Elevated sample results signal/cutoff (s/c) values when using eight (8) lots...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 30, 2020· Maquet Cardiovascular Us Sales, Llc

Recalled Item: Blood Monitoring Unit (BMU 40) Recalled by Maquet Cardiovascular Us Sales,...

The Issue: The Printed Circuit Board Assembly (PCBA) are not in compliance with the IEC...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 29, 2020· Verathon, Inc.

Recalled Item: BladderScan Prime Plus Probe - Product Usage: intended Recalled by Verathon,...

The Issue: Due to a change in handle material and process, probe handle may crack.

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 28, 2020· LivaNova USA Inc

Recalled Item: VNS Therapy¿ AspireSR¿ Generator Recalled by LivaNova USA Inc Due to Due to...

The Issue: Due to an extra digit being inadvertently added to the serial number of a...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 26, 2020· Advanced Bionics, LLC

Recalled Item: AB PowerCel 170 (velvet black) Recalled by Advanced Bionics, LLC Due to...

The Issue: Mislabeling; It has been determined that some batteries were improperly...

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

Class III — Low RiskOngoing