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. 2,576 recalls have been distributed to Idaho in the last 12 months.
Showing 8001–8020 of 48,215 recalls
Recalled Item: Circle K Honey Roasted Peanuts Recalled by Mount Franklin Foods LLC DBA Azar...
The Issue: Potential to contain undeclared soy and/or wheat allergen due to mislabeling.
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: 1. Circle K Get Up Trail Mix Recalled by Mount Franklin Foods LLC DBA Azar...
The Issue: Potential to contain undeclared soy and/or wheat allergen due to mislabeling.
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Circle K Sweet & Spicy Mix Recalled by Mount Franklin Foods LLC DBA Azar Nut...
The Issue: Potential to contain undeclared soy and/or wheat allergen due to mislabeling.
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Procedure pack: Presource PBDS Cat. PLMHCSBHF Recalled by Cardinal Health...
The Issue: Packs contain recalled components (equipment drapes, table cover, and...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Procedure pack: Presource PBDS Recalled by Cardinal Health 200, LLC Due to...
The Issue: Packs contain recalled components (equipment drapes, table cover, and...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Medfusion Syringe Pump Recalled by Smiths Medical ASD Inc. Due to A force...
The Issue: A force sensor in the occlusion detector may drift out of calibration...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Medfusion Syringe Pump Recalled by Smiths Medical ASD Inc. Due to A force...
The Issue: A force sensor in the occlusion detector may drift out of calibration...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Medfusion Syringe Pump Recalled by Smiths Medical ASD Inc. Due to A force...
The Issue: A force sensor in the occlusion detector may drift out of calibration...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Procedure packs: (1) Presource Pain Tray Recalled by Cardinal Health 200,...
The Issue: Packs contain recalled components (equipment drapes, table cover, and...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Procedure packs: (1) Presource PBDS Cat. PN33BPCR2 Recalled by Cardinal...
The Issue: XXX
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Medfusion Syringe Pump Recalled by Smiths Medical ASD Inc. Due to A force...
The Issue: A force sensor in the occlusion detector may drift out of calibration...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Procedure packs: (1) Presource PBDS Recalled by Cardinal Health 200, LLC Due...
The Issue: Packs contain recalled components (equipment drapes, table cover, and...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Presource Fistulogram Pack Recalled by Cardinal Health 200, LLC Due to Packs...
The Issue: Packs contain recalled components (equipment drapes, table cover, and...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Procedure packs: (1) Presource PBDS Recalled by Cardinal Health 200, LLC Due...
The Issue: Packs contain recalled components (equipment drapes, table cover, and...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Medfusion ASSEMBLY PLUNGER CASE LEFT 1/EA Recalled by Smiths Medical ASD...
The Issue: A force sensor in the occlusion detector may drift out of calibration...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Procedure packs: (1) Presource PBDS Cat. PNVMNIB21 Recalled by Cardinal...
The Issue: Packs contain recalled components (equipment drapes, table cover, and...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Procedure packs: (1) Presource Portacath Pack Recalled by Cardinal Health...
The Issue: Packs contain recalled components (equipment drapes, table cover, and...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Medfusion PLUNGER FLOAT PLATE Recalled by Smiths Medical ASD Inc. Due to A...
The Issue: A force sensor in the occlusion detector may drift out of calibration...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Procedure packs: (1) Presource PBDS Cat. PG33BTO21 Recalled by Cardinal...
The Issue: Packs contain recalled components (equipment drapes, table cover, and...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Semaglutide/Cyanocobalamin 2mg/0.4mg/mL Recalled by TMC Acquisitions LLC dba...
The Issue: Lack of Assurance of Sterility
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.