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. 2,588 recalls have been distributed to Idaho in the last 12 months.

48,215 total recalls
2,588 in last 12 months

Showing 63016320 of 48,215 recalls

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· 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· 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· 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· 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· 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
FoodMarch 4, 2024· Natural Waters of Viti Limited

Recalled Item: Fiji Natural Artesian Water 500 mL (24 pack) Case Recalled by Natural Waters...

The Issue: Firm testing revealed Manganese in addition to three bacterial genera.

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

Class III — Low RiskOngoing
Refund
DrugMarch 4, 2024· Par Sterile Products LLC

Recalled Item: Treprostinil Injection Recalled by Par Sterile Products LLC Due to Presence...

The Issue: Presence of Particulate Matter.

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

Class I — Serious Health HazardOngoing
Refund
DrugMarch 4, 2024· Novitium Pharma LLC

Recalled Item: Digoxin Tablets Recalled by Novitium Pharma LLC Due to Cross Contamination...

The Issue: Cross Contamination with Other Products:(mycophenolate mofetil).

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

Class III — Low RiskOngoing
Refund
DrugMarch 4, 2024· SUN PHARMACEUTICAL INDUSTRIES INC

Recalled Item: Febuxostat Tablets 80mg Recalled by SUN PHARMACEUTICAL INDUSTRIES INC Due to...

The Issue: CGMP Deviations: Microbial contamination was reported in stagnant water in...

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

Class II — Potential Health HazardOngoing
Refund
DrugMarch 4, 2024· SUN PHARMACEUTICAL INDUSTRIES INC

Recalled Item: Febuxostat Tablets 40mg Recalled by SUN PHARMACEUTICAL INDUSTRIES INC Due to...

The Issue: CGMP Deviations: Microbial contamination was reported in stagnant water in...

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

Class II — Potential Health HazardOngoing
Refund
Medical DeviceMarch 4, 2024· Avanos Medical, Inc.

Recalled Item: NEOMED* Pharmacy Syringes - Nonsterile (Non ENFit) with below product...

The Issue: The expiration date was not printed on the outer shipping label, leading to...

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

Class III — Low RiskOngoing
Medical DeviceMarch 4, 2024· Avanos Medical, Inc.

Recalled Item: NEOMED* Pharmacy Syringes - Nonsterile (Non ENFit) with below product...

The Issue: The expiration date was not printed on the outer shipping label, leading to...

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

Class III — Low RiskOngoing
Medical DeviceMarch 4, 2024· Avanos Medical, Inc.

Recalled Item: NEOMED* Pharmacy Syringes - Nonsterile (Non ENFit) with below product...

The Issue: The expiration date was not printed on the outer shipping label, leading to...

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

Class III — Low RiskOngoing
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
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: 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 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