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. 1,073 recalls have been distributed to Idaho in the last 12 months.

48,215 total recalls
1,073 in last 12 months

Showing 7621–7640 of 48,215 recalls

Medical DeviceOctober 4, 2023· Family Dollar Stores, Llc.

Recalled Item: AT HOME MARIJUANA TEST STRIP Recalled by Family Dollar Stores, Llc. Due to...

The Issue: Products were stored outside of labeled temperature requirements.

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 4, 2023· Family Dollar Stores, Llc.

Recalled Item: GOODSENSE DENTURE CLEANSER GRN TAB 40CT Recalled by Family Dollar Stores,...

The Issue: Products were stored outside of labeled temperature requirements.

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 4, 2023· Family Dollar Stores, Llc.

Recalled Item: CLEARBLUE SMART COUNTDOWN PRGNCY TST 1CT Recalled by Family Dollar Stores,...

The Issue: Products were stored outside of labeled temperature requirements.

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 4, 2023· Family Dollar Stores, Llc.

Recalled Item: DENTEMP ONE STEP .077OZ Recalled by Family Dollar Stores, Llc. Due to...

The Issue: Products were stored outside of labeled temperature requirements.

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 4, 2023· Family Dollar Stores, Llc.

Recalled Item: ORAL B MOUTH SORE RINSE 237ML Recalled by Family Dollar Stores, Llc. Due to...

The Issue: Products were stored outside of labeled temperature requirements.

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 4, 2023· Family Dollar Stores, Llc.

Recalled Item: ARC TEETH WHITENING PEN 0.06 FL OZ Recalled by Family Dollar Stores, Llc....

The Issue: Products were stored outside of labeled temperature requirements.

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 4, 2023· Edwards Lifesciences, LLC

Recalled Item: Acumen IQ Sensor Recalled by Edwards Lifesciences, LLC Due to Their is the...

The Issue: Their is the potential for flushing difficulties during setup of the...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 4, 2023· Edwards Lifesciences, LLC

Recalled Item: FloTrac Sensor with Vamp System Recalled by Edwards Lifesciences, LLC Due to...

The Issue: Their is the potential for flushing difficulties during setup of the...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 4, 2023· Edwards Lifesciences, LLC

Recalled Item: TruWave with Vamp System Pressure monitoring set Recalled by Edwards...

The Issue: Their is the potential for flushing difficulties during setup of the...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 4, 2023· Edwards Lifesciences, LLC

Recalled Item: FloTrac Sensor Recalled by Edwards Lifesciences, LLC Due to Their is the...

The Issue: Their is the potential for flushing difficulties during setup of the...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 4, 2023· Edwards Lifesciences, LLC

Recalled Item: TruWave Pressure monitoring set Recalled by Edwards Lifesciences, LLC Due to...

The Issue: Their is the potential for flushing difficulties during setup of the...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 4, 2023· Edwards Lifesciences, LLC

Recalled Item: Acumen IQ Sensor with VAMP System Recalled by Edwards Lifesciences, LLC Due...

The Issue: Their is the potential for flushing difficulties during setup of the...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 4, 2023· Family Dollar Stores, Llc.

Recalled Item: FIRST RESPONSE 2 CT Recalled by Family Dollar Stores, Llc. Due to Products...

The Issue: Products were stored outside of labeled temperature requirements.

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 4, 2023· Becton Dickinson Infusion Therapy Systems Inc.

Recalled Item: BD Insyte Autoguard BC Shielded IV Catheter with Blood Control Recalled by...

The Issue: Over-the-needle, intravascular catheters may have needles that do not...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 4, 2023· Family Dollar Stores, Llc.

Recalled Item: MEDIC's CHOICE CONTACT LENS SOLUTION 12FLOZ Recalled by Family Dollar...

The Issue: Products were stored outside of labeled temperature requirements.

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 3, 2023· Roche Diagnostics Operations, Inc.

Recalled Item: Tina-quant D-Dimer Test System Recalled by Roche Diagnostics Operations,...

The Issue: Elevated results were detected with Li-heparin plasma samples when compared...

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

Class II — Potential Health HazardOngoing
DrugOctober 3, 2023· Imprimis NJOF, LLC

Recalled Item: Epinephrine-Lidocaine HCl (0.25mg/mL and 7.5mg/mL) 1mL Single Use...

The Issue: Subpotent: Failing Test Results for Epinephrine

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

Class III — Low RiskOngoing
Refund
DrugOctober 2, 2023· Pine Pharmaceuticals, LLC

Recalled Item: Lidocaine-phenylephrine 1%-1.5% 1mL Single Dose Vial Recalled by Pine...

The Issue: Lack of Assurance of Sterility

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

Class II — Potential Health HazardOngoing
Refund
DrugOctober 2, 2023· Pine Pharmaceuticals, LLC

Recalled Item: Moxifloxacin in Balanced Salt Solution 400 mcg/0.4 mL (100 mcg/0.1 Recalled...

The Issue: Lack of Assurance of Sterility

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

Class II — Potential Health HazardOngoing
Refund
DrugOctober 2, 2023· Pine Pharmaceuticals, LLC

Recalled Item: TPC Drops (tropicamide 1%- phenylephrine 2.5%- cyclopentolate HCl 1%...

The Issue: Lack of Assurance of Sterility

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

Class II — Potential Health HazardOngoing
Refund