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. 987 recalls have been distributed to Alaska in the last 12 months.

46,762 total recalls
987 in last 12 months

Showing 18961–18980 of 46,762 recalls

Medical DeviceNovember 19, 2019· Angiodynamics, Inc.

Recalled Item: MICRO-PSD EXTERNAL BEAM PHOTON Recalled by Angiodynamics, Inc. Due to May...

The Issue: May result in readings outside of the expected accuracy range.

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 19, 2019· Angiodynamics, Inc.

Recalled Item: OARTRAC PROSTATE IMMOBILIZATION ENDORECTAL BALLOON DEVICE KIT Recalled by...

The Issue: May result in readings outside of the expected accuracy range.

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 19, 2019· Cardiac Assist, Inc

Recalled Item: TandemLife ECLS Procedure Kit - V24/A17 Recalled by Cardiac Assist, Inc Due...

The Issue: The kit contained a 29Fr ProtekDuo cannula instead of a 24Fr Protek Solo...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 19, 2019· Angiodynamics, Inc.

Recalled Item: MICRO-PSD Electron Recalled by Angiodynamics, Inc. Due to May result in...

The Issue: May result in readings outside of the expected accuracy range.

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 19, 2019· Angiodynamics, Inc.

Recalled Item: OARtrac PLUS CLINICAL DETECTOR UNIT Catalog Number: OTS-V2-Plus - Product...

The Issue: May result in readings outside of the expected accuracy range.

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

Class II — Potential Health HazardOngoing
DrugNovember 19, 2019· Baxter Healthcare Corporation

Recalled Item: 0.9% Sodium Chloride Irrigation USP 5000 mL bags Recalled by Baxter...

The Issue: Lack of Assurance of Sterility: Product has the potential to leak.

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

Class II — Potential Health HazardOngoing
Refund
Medical DeviceNovember 19, 2019· Siemens Healthcare Diagnostics, Inc.

Recalled Item: ADVIA Chemistry CardioPhase High Sensitivity C-Reactive Protein (hsCRP)...

The Issue: Atellica and ADVIA hsCRP calibrator accuracy has drifted away from the...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 19, 2019· Siemens Healthcare Diagnostics, Inc.

Recalled Item: Atellica CH High Sensitivity C-Reactive Protein (HsCRP) Calibrator - Product...

The Issue: Atellica CH: The Atellica¿ CH High Sensitivity CReactive Protein Calibrator...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 18, 2019· RAYSEARCH LABORATORIES AB

Recalled Item: RayStation stand-alone software treatment planning system Recalled by...

The Issue: Editing a static arc beam may unexpectedly set the MU of the beam to its...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 18, 2019· Boston Scientific Corporation

Recalled Item: Habib EUS RFA Recalled by Boston Scientific Corporation Due to During...

The Issue: During testing on the Habib EUS RFA device, a temperature increase was...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 18, 2019· Leica Microsystems, Inc.

Recalled Item: BOND Polymer Detection Kit Recalled by Leica Microsystems, Inc. Due to BOND...

The Issue: BOND Polymer Detection kits (DS9800) were held out of storage longer than...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 18, 2019· Diagnostica Stago, Inc.

Recalled Item: STA SYSTEM CONROL N + P (ref. 00678) Recalled by Diagnostica Stago, Inc. Due...

The Issue: A positive bias was confirmed to exists on the STA - Unicalibrator levels...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 18, 2019· Diagnostica Stago, Inc.

Recalled Item: STA UNICALIBRATOR (ref. 00675) Recalled by Diagnostica Stago, Inc. Due to A...

The Issue: A positive bias was confirmed to exists on the STA - Unicalibrator levels...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 18, 2019· Boston Scientific Corporation

Recalled Item: Habib EUS RFA Recalled by Boston Scientific Corporation Due to During...

The Issue: During testing on the Habib EUS RFA device, a temperature increase was...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 15, 2019· Arrow International Inc

Recalled Item: Arrow Berman Angiographic Catheter 60cm Item Number: AI-07130-J Recalled by...

The Issue: Potential leak in the balloon extension line. If a leak was present and went...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 15, 2019· Arrow International Inc

Recalled Item: Arrow Berman Angiographic Catheter 50cc Item Number: AI-07130 Recalled by...

The Issue: Potential leak in the balloon extension line. If a leak was present and went...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 15, 2019· Tosoh Smd Inc

Recalled Item: AIA-PACK B12 Pretreatment Set- IVD for diagnostic use for pre-treatment...

The Issue: The AIA-2000 bar code scanners depend on the quiet zone to help identify the...

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

Class III — Low RiskOngoing
FoodNovember 15, 2019· THE KRAFT HEINZ COMPANY

Recalled Item: Breakstones 4% Milkfat Large Curd Cottage Cheese Recalled by THE KRAFT HEINZ...

The Issue: Potential presence of pieces of red plastic and metal that may have been...

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

Class II — Potential Health HazardOngoing
Refund
FoodNovember 15, 2019· THE KRAFT HEINZ COMPANY

Recalled Item: Breakstones 4% Milkfat Small Curd Cottage Cheese Recalled by THE KRAFT HEINZ...

The Issue: Potential presence of pieces of red plastic and metal that may have been...

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

Class II — Potential Health HazardOngoing
Refund
FoodNovember 15, 2019· THE KRAFT HEINZ COMPANY

Recalled Item: Breakstones 2% Milkfat Lowfat Large Curd Cottage Cheese Recalled by THE...

The Issue: Potential presence of pieces of red plastic and metal that may have been...

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

Class II — Potential Health HazardOngoing
Refund