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. 2,017 recalls have been distributed to Idaho in the last 12 months.

48,215 total recalls
2,017 in last 12 months

Showing 67416760 of 48,215 recalls

DrugJanuary 10, 2024· BE PHARMACEUTICALS AG

Recalled Item: Fosaprepitant for Injection 150 mg per vial Recalled by BE PHARMACEUTICALS...

The Issue: Lack of Sterility Assurance: Aseptic process simulation failure.

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

Class II — Potential Health HazardOngoing
Refund
FoodJanuary 10, 2024· Now Foods

Recalled Item: Protocol for Life Balance Recalled by Now Foods Due to Amount of...

The Issue: Amount of Phosphatidyl Serine in product is less than stated on the label

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

Class III — Low RiskOngoing
Refund
DrugJanuary 10, 2024· MEDLINE INDUSTRIES, LP - Northfield

Recalled Item: Medline Remedy Clinical TREAT Antifungal Cream Recalled by MEDLINE...

The Issue: Labeling: Not Elsewhere Classified; Product labeling contains the claim of...

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

Class II — Potential Health HazardOngoing
Refund
Medical DeviceJanuary 9, 2024· Mckesson Medical-Surgical Inc. Corporate Office

Recalled Item: Abbott Rapid Dx N America LLC Reproductive Endocrinology Control Set...

The Issue: Facility Critical Temperature Excursions on 08-JAN 2024 in Walk-In due to...

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 9, 2024· Mckesson Medical-Surgical Inc. Corporate Office

Recalled Item: Abbott Point of Care Control Control i-STAT¿ Level 3 1.7 mL Recalled by...

The Issue: Facility Critical Temperature Excursions on 08-JAN 2024 in Walk-In due to...

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 9, 2024· Mckesson Medical-Surgical Inc. Corporate Office

Recalled Item: Steris Corporation Endo Cleaning Indicator VERIFY" RESITEST" Recalled by...

The Issue: Facility Critical Temperature Excursions on 08-JAN 2024 in Walk-In due to...

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 9, 2024· Aesculap Inc

Recalled Item: DISP.HASSON TROCAR 12/110MM Recalled by Aesculap Inc Due to The sterile...

The Issue: The sterile blister packaging may be damaged, and sterility may be compromised.

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 9, 2024· Mckesson Medical-Surgical Inc. Corporate Office

Recalled Item: Sekisui Diagnostics Control Kit OSOM¿ BVBLUE¿ Bacterial Vaginosis Recalled...

The Issue: Facility Critical Temperature Excursions on 08-JAN 2024 in Walk-In due to...

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 9, 2024· Aesculap Inc

Recalled Item: DISP.TROCAR W. DILATING PIN 10/110MM Recalled by Aesculap Inc Due to The...

The Issue: The sterile blister packaging may be damaged, and sterility may be compromised.

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 9, 2024· Aesculap Inc

Recalled Item: DISP.HASSON TROCAR 10/110MM Recalled by Aesculap Inc Due to The sterile...

The Issue: The sterile blister packaging may be damaged, and sterility may be compromised.

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 9, 2024· Aesculap Inc

Recalled Item: DISP.TROCAR W.DILATING PIN 12/110MM Recalled by Aesculap Inc Due to The...

The Issue: The sterile blister packaging may be damaged, and sterility may be compromised.

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 9, 2024· Mckesson Medical-Surgical Inc. Corporate Office

Recalled Item: Abbott Point of Care Control Control i-STAT¿ Level 1 10 X 1.7 mL Recalled by...

The Issue: Facility Critical Temperature Excursions on 08-JAN 2024 in Walk-In due to...

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 9, 2024· Aesculap Inc

Recalled Item: DISP.TROCAR W.DILATING PIN 12/110MM Recalled by Aesculap Inc Due to The...

The Issue: The sterile blister packaging may be damaged, and sterility may be compromised.

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 9, 2024· Silex Medical, LLC

Recalled Item: Signature Laparoscopic Instruments Recalled by Silex Medical, LLC Due to...

The Issue: Insulation on the tube did not extend fully to the proximal end of the shaft...

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 9, 2024· Silex Medical, LLC

Recalled Item: Signature Laparoscopic Instruments Recalled by Silex Medical, LLC Due to...

The Issue: Insulation on the tube did not extend fully to the proximal end of the shaft...

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 9, 2024· Silex Medical, LLC

Recalled Item: Signature Laparoscopic Instruments Recalled by Silex Medical, LLC Due to...

The Issue: Insulation on the tube did not extend fully to the proximal end of the shaft...

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 9, 2024· Silex Medical, LLC

Recalled Item: Signature Laparoscopic Instruments Recalled by Silex Medical, LLC Due to...

The Issue: Insulation on the tube did not extend fully to the proximal end of the shaft...

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 9, 2024· Silex Medical, LLC

Recalled Item: Signature Laparoscopic Instruments Recalled by Silex Medical, LLC Due to...

The Issue: Insulation on the tube did not extend fully to the proximal end of the shaft...

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 9, 2024· Silex Medical, LLC

Recalled Item: Signature Laparoscopic Instruments Recalled by Silex Medical, LLC Due to...

The Issue: Insulation on the tube did not extend fully to the proximal end of the shaft...

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 9, 2024· Silex Medical, LLC

Recalled Item: Signature Laparoscopic Instruments Recalled by Silex Medical, LLC Due to...

The Issue: Insulation on the tube did not extend fully to the proximal end of the shaft...

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

Class II — Potential Health HazardOngoing