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. 2,567 recalls have been distributed to Idaho in the last 12 months.

48,215 total recalls
2,567 in last 12 months

Showing 1138111400 of 48,215 recalls

FoodJuly 22, 2022· NATURE'S SUNSHINE PRODUCTS

Recalled Item: Aivia Whey Protein+ Power Herbs Chocolate Recalled by NATURE'S SUNSHINE...

The Issue: Label declares Whey but does not declare Milk.

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

Class II — Potential Health HazardOngoing
Refund
Medical DeviceJuly 22, 2022· Maquet Medical Systems USA

Recalled Item: BEQ-HLS 5050 USA Recalled by Maquet Medical Systems USA Due to The firm has...

The Issue: The firm has expanded the recall for the HLS Set Advanced regarding a...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 22, 2022· Maquet Medical Systems USA

Recalled Item: BEQ-HLS 7050 USA Recalled by Maquet Medical Systems USA Due to The firm has...

The Issue: The firm has expanded the recall for the HLS Set Advanced regarding a...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 22, 2022· Maquet Medical Systems USA

Recalled Item: BEQ-HLS 7050 USA Recalled by Maquet Medical Systems USA Due to The firm has...

The Issue: The firm has expanded the recall for the HLS Set Advanced regarding a...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 22, 2022· Maquet Medical Systems USA

Recalled Item: BEQ-HLS 5050 USA Recalled by Maquet Medical Systems USA Due to The firm has...

The Issue: The firm has expanded the recall for the HLS Set Advanced regarding a...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 22, 2022· Baxter Healthcare Corporation

Recalled Item: Baxter DISCPAC Syringe Tip Caps Recalled by Baxter Healthcare Corporation...

The Issue: There is a potential of the packaging not maintaining a sterile barrier for...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 22, 2022· Baxter Healthcare Corporation

Recalled Item: Baxter DISCPAC Syringe Tip Caps Recalled by Baxter Healthcare Corporation...

The Issue: There is a potential of the packaging not maintaining a sterile barrier for...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 22, 2022· Baxter Healthcare Corporation

Recalled Item: Baxter DISCPAC Syringe Tip Caps Recalled by Baxter Healthcare Corporation...

The Issue: There is a potential of the packaging not maintaining a sterile barrier for...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 22, 2022· Baxter Healthcare Corporation

Recalled Item: Baxter DISCPAC Syringe Tip Caps Recalled by Baxter Healthcare Corporation...

The Issue: There is a potential of the packaging not maintaining a sterile barrier for...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 22, 2022· Baxter Healthcare Corporation

Recalled Item: Baxter DISCPAC Syringe Tip Caps Recalled by Baxter Healthcare Corporation...

The Issue: There is a potential of the packaging not maintaining a sterile barrier for...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 22, 2022· Baxter Healthcare Corporation

Recalled Item: Baxter DISCPAC Syringe Tip Caps Recalled by Baxter Healthcare Corporation...

The Issue: There is a potential of the packaging not maintaining a sterile barrier for...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 22, 2022· Baxter Healthcare Corporation

Recalled Item: Baxter DISCPAC Syringe Tip Caps Recalled by Baxter Healthcare Corporation...

The Issue: There is a potential of the packaging not maintaining a sterile barrier for...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 22, 2022· Corin Ltd

Recalled Item: Corin METAFIX HIP STEM Recalled by Corin Ltd Due to One MetaFix size 7...

The Issue: One MetaFix size 7 collarless stem from batch 478179 which was incorrectly...

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

Class II — Potential Health HazardOngoing
DrugJuly 21, 2022· Teva Pharmaceuticals USA Inc

Recalled Item: Matzim LA (Diltiazem Hydrochloride) Extended-Release Tablets Recalled by...

The Issue: Failed Dissolution Specifications: below specification limits for dissolution.

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

Class II — Potential Health HazardOngoing
Refund
DrugJuly 21, 2022· Teva Pharmaceuticals USA Inc

Recalled Item: Matzim LA (Diltiazem Hydrochloride) Extended-Release Tablets Recalled by...

The Issue: Failed Dissolution Specifications: below specification limits for dissolution.

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

Class II — Potential Health HazardOngoing
Refund
DrugJuly 21, 2022· Ultra Supplement LLC

Recalled Item: SUSTANGO (Pendenadril Tytrate Blend) Capsules Recalled by Ultra Supplement...

The Issue: Marketed Without an Approved NDA/ANDA: Analytical testing showed the...

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

Class I — Serious Health HazardOngoing
Refund
FoodJuly 21, 2022· Vitamin Cottage Natural Food Markets, Inc.

Recalled Item: Amaranth Grain Organic Recalled by Vitamin Cottage Natural Food Markets,...

The Issue: Potential to be contaminated with Salmonella

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

Class II — Potential Health HazardOngoing
Refund
Medical DeviceJuly 21, 2022· Cardiac Assist, Inc

Recalled Item: TANDEM LIFE LivaNova LIFESPARC Controller Recalled by Cardiac Assist, Inc...

The Issue: Critical Failure of the LifeSPARC controller when the software freezes or...

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

Class I — Serious Health HazardOngoing
Medical DeviceJuly 21, 2022· Medline Industries Inc.

Recalled Item: Medline CHEST TUBE REORDER NO: DYNJ36762A Recalled by Medline Industries...

The Issue: Due to a non-sterile component (tape) being place within the sterile portion...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 21, 2022· Getinge Usa Sales Inc

Recalled Item: Servo-air Ventilator System-The Servo-air Ventilator System is: Intended for...

The Issue: Device does not meet regulatory requirements of stability while stationary,...

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

Class II — Potential Health HazardOngoing