Product Recalls in Idaho

Product recalls affecting Idaho — including food, drugs, consumer products, medical devices, and vehicles distributed to Idaho. RecallDetector monitors distribution data from the FDA, USDA, CPSC, and NHTSA to show you which recalls are relevant to your area. 2,594 recalls have been distributed to Idaho in the last 12 months.

48,215 total recalls
2,594 in last 12 months

Showing 44814500 of 27,833 recalls

Medical DeviceMarch 6, 2024· Exactech, Inc.

Recalled Item: Exactech Equinoxe REVERSE SHOULDER Recalled by Exactech, Inc. Due to The...

The Issue: The packaging of these affected UHMWPE humeral liners and glenoids are...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 6, 2024· Exactech, Inc.

Recalled Item: Exactech Equinoxe GLENOID Recalled by Exactech, Inc. Due to The packaging of...

The Issue: The packaging of these affected UHMWPE humeral liners and glenoids are...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 6, 2024· Exactech, Inc.

Recalled Item: Exactech Equinoxe REVERSE SHOULDER Recalled by Exactech, Inc. Due to The...

The Issue: The packaging of these affected UHMWPE humeral liners and glenoids are...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 6, 2024· Exactech, Inc.

Recalled Item: Exactech Equinoxe GLENOID Recalled by Exactech, Inc. Due to The packaging of...

The Issue: The packaging of these affected UHMWPE humeral liners and glenoids are...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 6, 2024· Outset Medical, Inc.

Recalled Item: Tablo Hemodialysis System Recalled by Outset Medical, Inc. Due to...

The Issue: Hemodialysis System, pre and post dialyzer peroxide-cured silicone tubing,...

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

Class I — Serious Health HazardOngoing
Medical DeviceMarch 5, 2024· Tandem Diabetes Care, Inc.

Recalled Item: t:connect mobile app used in conjunction with t:slim X2 insulin Recalled by...

The Issue: During normal use, the mobile app version 2.7 may crash and be automatically...

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

Class I — Serious Health HazardOngoing
Medical DeviceMarch 5, 2024· Quidel Corporation

Recalled Item: QUIDEL InflammaDry MMP-9 Test Recalled by Quidel Corporation Due to There...

The Issue: There are two windows on the test device, the control line window and the...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 5, 2024· Beckman Coulter, Inc.

Recalled Item: DxI 9000 Access Immunoassay Analyzer Recalled by Beckman Coulter, Inc. Due...

The Issue: Beckman Coulter manufacturing discovered cracks around a threaded insert on...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 5, 2024· Unomedical A/S

Recalled Item: Neria Soft Infusion Set Recalled by Unomedical A/S Due to Specific lots of...

The Issue: Specific lots of Neria Soft Infusion Sets, which have been shipped into the...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 5, 2024· Quidel Corporation

Recalled Item: QUIDEL InflammaDry MMP-9 Test Recalled by Quidel Corporation Due to There...

The Issue: There are two windows on the test device, the control line window and the...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 5, 2024· Randox Laboratories Ltd.

Recalled Item: Clinical Chemistry Calibration Serum (Catalog number Cal2351) that is 20x5ml...

The Issue: Randox Laboratories has identified that Inorganic Phosphate in Calibration...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 5, 2024· MEDLINE INDUSTRIES, LP - Northfield

Recalled Item: Bed Assist Bars Recalled by MEDLINE INDUSTRIES, LP - Northfield Due to...

The Issue: Medline is recalling certain lots of our Adult Portable Bed Rails that were...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 5, 2024· MEDLINE INDUSTRIES, LP - Northfield

Recalled Item: Bed Assist Bars Recalled by MEDLINE INDUSTRIES, LP - Northfield Due to...

The Issue: Medline is recalling certain lots of our Adult Portable Bed Rails that were...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 5, 2024· Baxter Healthcare Corporation

Recalled Item: Hill-Rom PRO+ 36" MRS Surface Recalled by Baxter Healthcare Corporation Due...

The Issue: Inconsistencies were identified with service records associated with...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 4, 2024· Qiagen Sciences LLC

Recalled Item: EZ2 Connect MDx-IVD Designed to perform automated isolation and purification...

The Issue: Insufficient welding leads to the heater cable becoming brittle and present...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 4, 2024· Abbott GmbH

Recalled Item: Alinity i Anti-HCV Reagent Kit Recalled by Abbott GmbH Due to Customer...

The Issue: Customer complaints were received regarding falsely elevated results for...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 4, 2024· Abbott GmbH

Recalled Item: ARCHITECT Anti-HCV Reagent Kit Recalled by Abbott GmbH Due to Customer...

The Issue: Customer complaints were received regarding falsely elevated results for...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 4, 2024· X-NAV Technologies, LLC

Recalled Item: X-Guide Handpiece Adaptor Sleeve 1 Recalled by X-NAV Technologies, LLC Due...

The Issue: The Handpiece Adaptor may have a manufacturing defect causing incorrect...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 4, 2024· X-NAV Technologies, LLC

Recalled Item: X-Guide Handpiece Adaptor Sleeve 3 Recalled by X-NAV Technologies, LLC Due...

The Issue: The Handpiece Adaptor may have a manufacturing defect causing incorrect...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 4, 2024· Ion Beam Applications S.A.

Recalled Item: IBA Proton Therapy System - PROTEUS 235 Recalled by Ion Beam Applications...

The Issue: There is a risk of mistreatment as irradiation is not prevented when some...

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

Class II — Potential Health HazardOngoing