Product Recalls in South Dakota

Product recalls affecting South Dakota — including food, drugs, consumer products, medical devices, and vehicles distributed to South Dakota. RecallDetector monitors distribution data from the FDA, USDA, CPSC, and NHTSA to show you which recalls are relevant to your area. 2,516 recalls have been distributed to South Dakota in the last 12 months.

47,632 total recalls
2,516 in last 12 months

Showing 74217440 of 47,632 recalls

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 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 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: 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· 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 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· 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· 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: 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· St. Jude Medical

Recalled Item: CardioMEMS Patient Electronic System (PES) Recalled by St. Jude Medical Due...

The Issue: Potential for damaged and frayed power connector plug with repeated bending...

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: 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: FIXODENT ORG CREAM 2.4OZ 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: VERIQUICK PREGNANCY TEST 1CT 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· Baxter Healthcare Corporation

Recalled Item: HILLROM PROGRESSA+ BED Recalled by Baxter Healthcare Corporation Due to...

The Issue: Progressa+ beds have the potential for static buildup from the casters...

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
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 2, 2023· Pfizer Inc.

Recalled Item: 2% Lidocaine HCl Injection Recalled by Pfizer Inc. Due to Presence of...

The Issue: Presence of Particulate Matter: identified as glass.

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

Class I — Serious Health HazardOngoing
Refund
DrugOctober 2, 2023· Pfizer Inc.

Recalled Item: 4.2% Sodium Bicarbonate Injection Recalled by Pfizer Inc. Due to Presence of...

The Issue: Presence of Particulate Matter: identified as glass.

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

Class I — Serious Health HazardOngoing
Refund
DrugOctober 2, 2023· Pfizer Inc.

Recalled Item: 1% Lidocaine HCl Injection Recalled by Pfizer Inc. Due to Presence of...

The Issue: Presence of Particulate Matter: identified as glass.

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

Class I — Serious Health HazardOngoing
Refund