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 62616280 of 48,215 recalls

Medical DeviceMarch 11, 2024· Conformis, Inc.

Recalled Item: Identity Imprint PS Tibial Tray Size 4: Lot 540287 Recalled by Conformis,...

The Issue: Size 5 Tibial Tray from Lot 508287 was packaged in a Size 4 box from Lot...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 11, 2024· Baxter Healthcare Corporation

Recalled Item: HDS Traction Boot II Recalled by Baxter Healthcare Corporation Due to Baxter...

The Issue: Baxter Healthcare Corporation is issuing an Urgent Medical Device Recall for...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 9, 2024· Noah Medical

Recalled Item: Galaxy System (specifically GAL-019 Recalled by Noah Medical Due to Due to a...

The Issue: Due to a misaligned calibration of the wired controller that may result in...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 7, 2024· Olympus Corporation of the Americas

Recalled Item: POWERSEAL 5 mm Recalled by Olympus Corporation of the Americas Due to Upon...

The Issue: Upon initial activation of the seal function, the POWERSEAL non-conformance...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 7, 2024· Olympus Corporation of the Americas

Recalled Item: POWERSEAL 5 mm Recalled by Olympus Corporation of the Americas Due to Upon...

The Issue: Upon initial activation of the seal function, the POWERSEAL non-conformance...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 7, 2024· Olympus Corporation of the Americas

Recalled Item: POWERSEAL 5 mm Recalled by Olympus Corporation of the Americas Due to Upon...

The Issue: Upon initial activation of the seal function, the POWERSEAL non-conformance...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 7, 2024· Fresenius Kabi USA, LLC

Recalled Item: LVP Software of the Ivenix Infusion System (IIS) Recalled by Fresenius Kabi...

The Issue: Software has anomalies that have the potential to cause underdose, overdose,...

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

Class I — Serious Health HazardOngoing
FoodMarch 7, 2024· Stonewall Kitchen, LLC

Recalled Item: Stonewall Kitchen Cinnamon Sugar Doughnut Mix Recalled by Stonewall Kitchen,...

The Issue: Product contains undeclared wheat.

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

Class I — Serious Health HazardOngoing
Refund
DrugMarch 7, 2024· Teva Pharmaceuticals USA, Inc

Recalled Item: Tri-Lo-Sprintec (norgestimate and ethinyl estradiol) tablets USP - triphasic...

The Issue: Failed Dissolution Specifications

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

Class II — Potential Health HazardOngoing
Refund
DrugMarch 6, 2024· B. Braun Medical Inc

Recalled Item: Potassium Chloride for Injection Concentrate USP Recalled by B. Braun...

The Issue: Lack of assurance of sterility: pinholes, within the blue label characters...

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

Class II — Potential Health HazardOngoing
Refund
FoodMarch 6, 2024· Colonna Brothers Inc.

Recalled Item: Supreme Tradition brand and Marcum brand ground cinnamon. Packaged in...

The Issue: Elevated lead levels in cinnamon

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

Class II — Potential Health HazardOngoing
Refund
Medical DeviceMarch 6, 2024· Exactech, Inc.

Recalled Item: Exactech Equinoxe REVERSE SHOULDER Recalled by Exactech, Inc. Due to The...

The Issue: The packaging of these affected UHMWPE humeral liners and glenoids are...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 6, 2024· Exactech, Inc.

Recalled Item: Exactech Equinoxe GLENOID Recalled by Exactech, Inc. Due to The packaging of...

The Issue: The packaging of these affected UHMWPE humeral liners and glenoids are...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 6, 2024· Artivion, Inc

Recalled Item: CryoValve SG Cryopreserved Pulmonary Human Heart Valve Recalled by Artivion,...

The Issue: The blood cultures performed as part of the organ donation process were...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 6, 2024· Exactech, Inc.

Recalled Item: Exactech Equinoxe Humeral Liner: Item Numbers: a) 320-40-00 Recalled by...

The Issue: The packaging of these affected UHMWPE humeral liners and glenoids are...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 6, 2024· Exactech, Inc.

Recalled Item: Exactech Equinoxe REVERSE SHOULDER Recalled by Exactech, Inc. Due to The...

The Issue: The packaging of these affected UHMWPE humeral liners and glenoids are...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 6, 2024· Exactech, Inc.

Recalled Item: Exactech Equinoxe GLENOID Recalled by Exactech, Inc. Due to The packaging of...

The Issue: The packaging of these affected UHMWPE humeral liners and glenoids are...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 6, 2024· Exactech, Inc.

Recalled Item: Exactech Equinoxe CAGE GLENOID Recalled by Exactech, Inc. Due to The...

The Issue: The packaging of these affected UHMWPE humeral liners and glenoids are...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 6, 2024· Exactech, Inc.

Recalled Item: Exactech Equinoxe CAGE GLENOID Recalled by Exactech, Inc. Due to The...

The Issue: The packaging of these affected UHMWPE humeral liners and glenoids are...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 6, 2024· Exactech, Inc.

Recalled Item: Exactech Equinoxe GLENOID Recalled by Exactech, Inc. Due to The packaging of...

The Issue: The packaging of these affected UHMWPE humeral liners and glenoids are...

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

Class II — Potential Health HazardOngoing