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. 1,030 recalls have been distributed to South Dakota in the last 12 months.

47,632 total recalls
1,030 in last 12 months

Showing 16101–16120 of 47,632 recalls

DrugDecember 17, 2020· SCA Pharmaceuticals

Recalled Item: fentaNYL 100 mcg/50mL Ropivacaine HCl 0.1% in 0.9% Sodium Chloride 50 mL...

The Issue: Lack of Assurance of Sterility; potential for a defective syringe cap,...

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

Class II — Potential Health HazardOngoing
Refund
DrugDecember 17, 2020· SCA Pharmaceuticals

Recalled Item: SUCcinylcholine Chloride 100 mg/5mL Recalled by SCA Pharmaceuticals Due to...

The Issue: Lack of Assurance of Sterility; potential for a defective syringe cap,...

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

Class II — Potential Health HazardOngoing
Refund
DrugDecember 17, 2020· SCA Pharmaceuticals

Recalled Item: PHENYLephrine HCl 5000 mg/50 mL in Sodium Chloride 0.9% (100 mcg/mL) Rx Only...

The Issue: Lack of Assurance of Sterility; potential for a defective syringe cap,...

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

Class II — Potential Health HazardOngoing
Refund
DrugDecember 17, 2020· SCA Pharmaceuticals

Recalled Item: ePHEDrine Sulfate 50 mg/10mL in 0.9% Sodium Chloride Injection Recalled by...

The Issue: Lack of Assurance of Sterility; potential for a defective syringe cap,...

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

Class II — Potential Health HazardOngoing
Refund
DrugDecember 17, 2020· SCA Pharmaceuticals

Recalled Item: HYDROmorphone HCl 10mg/50mL in 0.9% Sodium Chloride Injection Recalled by...

The Issue: Lack of Assurance of Sterility; potential for a defective syringe cap,...

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

Class II — Potential Health HazardOngoing
Refund
DrugDecember 17, 2020· SCA Pharmaceuticals

Recalled Item: Esmolol HCl 100 mg/10 mL (10mg/ mL) Recalled by SCA Pharmaceuticals Due to...

The Issue: Lack of Assurance of Sterility; potential for a defective syringe cap,...

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

Class II — Potential Health HazardOngoing
Refund
DrugDecember 17, 2020· SCA Pharmaceuticals

Recalled Item: ePHEDrine Sulfate Recalled by SCA Pharmaceuticals Due to Lack of Assurance...

The Issue: Lack of Assurance of Sterility; potential for a defective syringe cap,...

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

Class II — Potential Health HazardOngoing
Refund
DrugDecember 17, 2020· SCA Pharmaceuticals

Recalled Item: morphine sulfate 150 mg/30 mL in 0.9% Sodium Chloride Injection Recalled by...

The Issue: Lack of Assurance of Sterility; potential for a defective syringe cap,...

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

Class II — Potential Health HazardOngoing
Refund
DrugDecember 17, 2020· NDAL Mfg Inc.

Recalled Item: ManukaGuard Medical Grade Manuka Honey Allercleanse Nasal Spray Recalled by...

The Issue: Microbial Contamination of Non-Sterile Products: Product confirmed to have yeast

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

Class I — Serious Health HazardOngoing
Refund
DrugDecember 16, 2020· US Compounding Inc

Recalled Item: Succinylcholine Chloride PF Inj. 200 mg/10 mL Recalled by US Compounding Inc...

The Issue: Labeling: Incorrect or Missing lot and/or expiration date: The lot number...

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

Class III — Low RiskOngoing
Refund
Medical DeviceDecember 16, 2020· Medtronic Neurosurgery

Recalled Item: X1 Recalled by Medtronic Neurosurgery Due to Neonatal Valves were...

The Issue: Neonatal Valves were manufactured with a ventricular catheter connection...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 16, 2020· Medtronic Neurosurgery

Recalled Item: X1 Recalled by Medtronic Neurosurgery Due to Neonatal Valves were...

The Issue: Neonatal Valves were manufactured with a ventricular catheter connection...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 16, 2020· Medtronic Neurosurgery

Recalled Item: X1 Recalled by Medtronic Neurosurgery Due to Neonatal Valves were...

The Issue: Neonatal Valves were manufactured with a ventricular catheter connection...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 16, 2020· Microbiologics Inc

Recalled Item: KWIK-STIK 2 Pack Recalled by Microbiologics Inc Due to Contamination with S....

The Issue: Contamination with S. epidermidis

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 16, 2020· Microbiologics Inc

Recalled Item: KWIK-STI(TM) Recalled by Microbiologics Inc Due to The expiration date on...

The Issue: The expiration date on the label of one component (negative control 0243U)...

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

Class III — Low RiskOngoing
Medical DeviceDecember 16, 2020· Cook Medical Llc

Recalled Item: Disposable Humidification Flask Recalled by Cook Medical Llc Due to A small...

The Issue: A small percentage of the Disposable Humidification Flasks may have a...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 15, 2020· Wahl Clipper Corp

Recalled Item: WAHL 4212 HEATED MASSAGER Recalled by Wahl Clipper Corp Due to The...

The Issue: The connection between the massager and heat element can overheat causing...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 15, 2020· Ortho Clinical Diagnostics Inc

Recalled Item: VITROS Chemistry Products TP Slides- IVD measure total protein (TP) Recalled...

The Issue: Eltrombopag Interference for VITROS Chemistry Products TP Slides and VITROS...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 15, 2020· DePuy Orthopaedics, Inc.

Recalled Item: Pinnacle Cups Recalled by DePuy Orthopaedics, Inc. Due to Certain Pinnacle...

The Issue: Certain Pinnacle Cup devices may potentially exhibit an oversized "minor...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 15, 2020· Penumbra Inc.

Recalled Item: Penumbra JET 7MAX KIT Penumbra JET 7 Reperfusion Catheter+ MAX Recalled by...

The Issue: The catheter may become susceptible to distal tip damage during use. Distal...

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

Class I — Serious Health HazardOngoing