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. 1,001 recalls have been distributed to Idaho in the last 12 months.

48,215 total recalls
1,001 in last 12 months

Showing 23101–23120 of 48,215 recalls

FoodJanuary 4, 2019· Diamond Crystal Brands, Inc.

Recalled Item: Chef's Companion Chocolate Instant Pudding & Pie Filling Recalled by Diamond...

The Issue: Recalled products were manufactured with an ingredient that is potentially...

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

Class I — Serious Health HazardOngoing
Refund
FoodJanuary 4, 2019· Diamond Crystal Brands, Inc.

Recalled Item: Chef's Companion Lemon Instant Pudding & Pie Filling Recalled by Diamond...

The Issue: Recalled products were manufactured with an ingredient that is potentially...

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

Class I — Serious Health HazardOngoing
Refund
FoodJanuary 4, 2019· Diamond Crystal Brands, Inc.

Recalled Item: Culinary Secrets Recalled by Diamond Crystal Brands, Inc. Due to Potential...

The Issue: Recalled products were manufactured with an ingredient that is potentially...

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

Class I — Serious Health HazardOngoing
Refund
FoodJanuary 4, 2019· Diamond Crystal Brands, Inc.

Recalled Item: Gordon Choice Recalled by Diamond Crystal Brands, Inc. Due to Potential...

The Issue: Recalled products were manufactured with an ingredient that is potentially...

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

Class I — Serious Health HazardOngoing
Refund
FoodJanuary 4, 2019· Diamond Crystal Brands, Inc.

Recalled Item: Cheesecake mix packaged in the following ways: 1) Chef's Companion Recalled...

The Issue: Recalled products were manufactured with an ingredient that is potentially...

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

Class I — Serious Health HazardOngoing
Refund
FoodJanuary 4, 2019· Ardent Mills, LLC

Recalled Item: MEMBERS MARK SELF RISE FLR 25LB Recalled by Ardent Mills, LLC Due to...

The Issue: Ardent Mills is voluntarily recalling certain lots of Self-Rising Flour...

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

Class II — Potential Health HazardOngoing
Refund
Medical DeviceJanuary 4, 2019· Cook Inc.

Recalled Item: Bentson PTFE Wire Guide Recalled by Cook Inc. Due to The wire guide may be...

The Issue: The wire guide may be incorrectly loaded into the wire guide holder, leading...

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 4, 2019· Cook Inc.

Recalled Item: Fixed Core Straight Safety Wire Guide Recalled by Cook Inc. Due to The wire...

The Issue: The wire guide may be incorrectly loaded into the wire guide holder, leading...

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 4, 2019· Cook Inc.

Recalled Item: Sof-Flex Multi-Lenqth Ureteral Stent Set Recalled by Cook Inc. Due to The...

The Issue: The wire guide may be incorrectly loaded into the wire guide holder, leading...

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 4, 2019· Cook Inc.

Recalled Item: Universa Soft Ureteral Stent Recalled by Cook Inc. Due to The wire guide may...

The Issue: The wire guide may be incorrectly loaded into the wire guide holder, leading...

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 4, 2019· Cook Inc.

Recalled Item: Percutaneous Pigtail Nephrostomy Set Recalled by Cook Inc. Due to The wire...

The Issue: The wire guide may be incorrectly loaded into the wire guide holder, leading...

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 4, 2019· Cook Inc.

Recalled Item: Percutaneous Malecot Nephrostomy Set Recalled by Cook Inc. Due to The wire...

The Issue: The wire guide may be incorrectly loaded into the wire guide holder, leading...

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 4, 2019· Cook Inc.

Recalled Item: Heavy Duty PTFE Wire Guide Recalled by Cook Inc. Due to The wire guide may...

The Issue: The wire guide may be incorrectly loaded into the wire guide holder, leading...

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 4, 2019· Cook Inc.

Recalled Item: Angled Tip Ureteral Catheter Set Recalled by Cook Inc. Due to The wire guide...

The Issue: The wire guide may be incorrectly loaded into the wire guide holder, leading...

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 4, 2019· Cook Inc.

Recalled Item: Roadrunner Hydrophilic PC Wire Guide Recalled by Cook Inc. Due to The wire...

The Issue: The wire guide may be incorrectly loaded into the wire guide holder, leading...

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 4, 2019· Cook Inc.

Recalled Item: Urethral Dilator Set Recalled by Cook Inc. Due to The wire guide may be...

The Issue: The wire guide may be incorrectly loaded into the wire guide holder, leading...

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 4, 2019· Cook Inc.

Recalled Item: Wire Guide Recalled by Cook Inc. Due to The wire guide may be incorrectly...

The Issue: The wire guide may be incorrectly loaded into the wire guide holder, leading...

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 4, 2019· Cook Inc.

Recalled Item: Kwart Retro-Inject Ureteral Stent Set Recalled by Cook Inc. Due to The wire...

The Issue: The wire guide may be incorrectly loaded into the wire guide holder, leading...

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 4, 2019· Cook Inc.

Recalled Item: Sof-Flex Double Pigtail Ureteral Stent Set Recalled by Cook Inc. Due to The...

The Issue: The wire guide may be incorrectly loaded into the wire guide holder, leading...

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 4, 2019· Cook Inc.

Recalled Item: Percutaneous Entry Set Recalled by Cook Inc. Due to The wire guide may be...

The Issue: The wire guide may be incorrectly loaded into the wire guide holder, leading...

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

Class II — Potential Health HazardOngoing