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. 2,528 recalls have been distributed to South Dakota in the last 12 months.

47,632 total recalls
2,528 in last 12 months

Showing 63216340 of 47,632 recalls

Medical DeviceFebruary 21, 2024· Bruder Healthcare Company, LLC

Recalled Item: Thermalon Stye Compress Recalled by Bruder Healthcare Company, LLC Due to...

The Issue: Thermalon and MediBeads moist heat compresses from certain lots may have...

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 21, 2024· Alcon Research, LLC

Recalled Item: SYRINGE Recalled by Alcon Research, LLC Due to Medline Bulb irrigation...

The Issue: Medline Bulb irrigation syringes recalled due to potential for packaging...

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 21, 2024· Bruder Healthcare Company, LLC

Recalled Item: Thermalon Neck Wrap Recalled by Bruder Healthcare Company, LLC Due to...

The Issue: Thermalon and MediBeads moist heat compresses from certain lots may have...

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 21, 2024· Puritan Medical Products Company, Llc

Recalled Item: HydroFlock Sterile Flocked Collection Device Recalled by Puritan Medical...

The Issue: It was discovered through a customer complaint that mislabeled product was...

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 21, 2024· Bruder Healthcare Company, LLC

Recalled Item: MediBeads Neck Wrap Recalled by Bruder Healthcare Company, LLC Due to...

The Issue: Thermalon and MediBeads moist heat compresses from certain lots may have...

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 21, 2024· Bruder Healthcare Company, LLC

Recalled Item: Thermalon Eye Compress Recalled by Bruder Healthcare Company, LLC Due to...

The Issue: Thermalon and MediBeads moist heat compresses from certain lots may have...

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 21, 2024· Bruder Healthcare Company, LLC

Recalled Item: MediBeads King Pad Recalled by Bruder Healthcare Company, LLC Due to...

The Issue: Thermalon and MediBeads moist heat compresses from certain lots may have...

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 21, 2024· Bruder Healthcare Company, LLC

Recalled Item: Thermalon Heating Pad Recalled by Bruder Healthcare Company, LLC Due to...

The Issue: Thermalon and MediBeads moist heat compresses from certain lots may have...

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 21, 2024· InfuTronix LLC

Recalled Item: Nimbus Administration Set Recalled by InfuTronix LLC Due to InfuTronix is...

The Issue: InfuTronix is removing the Nimbus Infusion Pump Systems from the market due...

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

Class I — Serious Health HazardOngoing
Medical DeviceFebruary 21, 2024· InfuTronix LLC

Recalled Item: Nimbus II Infusion System Recalled by InfuTronix LLC Due to InfuTronix is...

The Issue: InfuTronix is removing the Nimbus Infusion Pump Systems from the market due...

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

Class I — Serious Health HazardOngoing
Medical DeviceFebruary 21, 2024· Covidien

Recalled Item: Situate Laparotomy Sponge Recalled by Covidien Due to Packs including 5...

The Issue: Packs including 5 laparotomy sponges may contain incorrect product with a...

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

Class II — Potential Health HazardOngoing
DrugFebruary 20, 2024· Eugia US LLC

Recalled Item: Nicardipine Hydrochloride Injection Recalled by Eugia US LLC Due to Failed...

The Issue: Failed Impurities/Degradation Specifications: Out of specification for...

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

Class II — Potential Health HazardOngoing
Refund
DrugFebruary 20, 2024· Eugia US LLC

Recalled Item: Nicardipine Hydrochloride Injection (2.5mg/mL) Recalled by Eugia US LLC Due...

The Issue: Failed Impurities/Degradation Specifications: Out of specification for...

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

Class II — Potential Health HazardOngoing
Refund
DrugFebruary 20, 2024· Contract Pharmaceuticals Limited Canada

Recalled Item: Clindamycin Phosphate Recalled by Contract Pharmaceuticals Limited Canada...

The Issue: Defective Container: Out of specification for weight due to a slow leakage...

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

Class III — Low RiskOngoing
Refund
DrugFebruary 20, 2024· Contract Pharmaceuticals Limited Canada

Recalled Item: Clindamycin Phosphate Topical Solution USP Recalled by Contract...

The Issue: Defective Container: Out of specification for weight due to a slow leakage...

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

Class III — Low RiskOngoing
Refund
DrugFebruary 20, 2024· Denver Solutions, LLC DBA Leiters Health

Recalled Item: Moxifloxacin 5mg/ml Recalled by Denver Solutions, LLC DBA Leiters Health Due...

The Issue: Presence of Particulate Matter: glass vials from the manufacturer showed...

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

Class II — Potential Health HazardOngoing
Refund
DrugFebruary 20, 2024· Denver Solutions, LLC DBA Leiters Health

Recalled Item: Lidocaine HCL 1% (10mg/mL) Recalled by Denver Solutions, LLC DBA Leiters...

The Issue: Presence of Particulate Matter: glass vials from the manufacturer showed...

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

Class II — Potential Health HazardOngoing
Refund
DrugFebruary 20, 2024· Denver Solutions, LLC DBA Leiters Health

Recalled Item: Moxifloxacin PF Recalled by Denver Solutions, LLC DBA Leiters Health Due to...

The Issue: Presence of Particulate Matter: glass vials from the manufacturer showed...

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

Class II — Potential Health HazardOngoing
Refund
Medical DeviceFebruary 20, 2024· Boston Scientific Corporation

Recalled Item: EndoVive 20 Fr Safety PEG Push w/ENFit Kit (Box 2)-Indicated Recalled by...

The Issue: Inability to advance the guidewire through the feeding tube during placement...

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 20, 2024· Boston Scientific Corporation

Recalled Item: EndoVive 20Fr Push Standard PEG Kit w/ENFit (Box 2)-Indicated for Recalled...

The Issue: Inability to advance the guidewire through the feeding tube during placement...

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

Class II — Potential Health HazardOngoing