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. 2,373 recalls have been distributed to South Dakota in the last 12 months.

47,632 total recalls
2,373 in last 12 months

Showing 2214122160 of 47,632 recalls

DrugMarch 13, 2019· Advanced Pharma Inc.

Recalled Item: Glycopyrrolate 0.6 mg/3 mL (0.2 mg per mL) Injectable Solution Recalled by...

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
DrugMarch 13, 2019· Advanced Pharma Inc.

Recalled Item: 2% Lidocaine HCl Injectable Solution Recalled by Advanced Pharma Inc. Due to...

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
DrugMarch 13, 2019· Advanced Pharma Inc.

Recalled Item: Phenylephrine HCl Recalled by Advanced Pharma Inc. Due to Lack of Assurance...

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
DrugMarch 13, 2019· Advanced Pharma Inc.

Recalled Item: Midazolam Benzodiazepine 50 mg/50 mL (1 mg/mL) Injectable Solution 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
DrugMarch 13, 2019· Advanced Pharma Inc.

Recalled Item: Phenylephrine HCl Recalled by Advanced Pharma Inc. Due to Lack of Assurance...

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
DrugMarch 13, 2019· Advanced Pharma Inc.

Recalled Item: Heparin 10 Units/10 mL 10 Units in 0.45% Sodium Chloride Recalled by...

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
DrugMarch 13, 2019· Advanced Pharma Inc.

Recalled Item: HYDROmorphone HCl 1 mg in 0.9% Sodium Chloride Recalled by Advanced Pharma...

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
DrugMarch 13, 2019· Advanced Pharma Inc.

Recalled Item: Phenylephrine HCl Recalled by Advanced Pharma Inc. Due to Lack of Assurance...

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
DrugMarch 13, 2019· Advanced Pharma Inc.

Recalled Item: Neostigmine Methylsulfate Injection Solution 5 mg/5mL (1 mg per mL) 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
Medical DeviceMarch 13, 2019· Medical Components, Inc dba MedComp

Recalled Item: 14F x 24CM SLX Double Lumen Full Tray Hemodialysis catheter insertion kits...

The Issue: Tray label indicates the kits are packaged with a 15F "valved" peelable...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 13, 2019· Medical Components, Inc dba MedComp

Recalled Item: 14F x 20CM SLX Double Lumen Full Tray Hemodialysis catheter insertion kits...

The Issue: Tray label indicates the kits are packaged with a 15F "valved" peelable...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 13, 2019· Medical Components, Inc dba MedComp

Recalled Item: 14F x 30CM SLX Double Lumen Full Tray Hemodialysis catheter insertion kits...

The Issue: Tray label indicates the kits are packaged with a 15F "valved" peelable...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 13, 2019· Vyaire Medical

Recalled Item: enFlow Disposable Cartridge Recalled by Vyaire Medical Due to Testing has...

The Issue: Testing has demonstrated aluminum elution from the enFlow Disposable...

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

Class I — Serious Health HazardOngoing
Medical DeviceMarch 13, 2019· Vyaire Medical

Recalled Item: enFlow Disposable Cartridge with IV Extension Set Recalled by Vyaire Medical...

The Issue: Testing has demonstrated aluminum elution from the enFlow Disposable...

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

Class I — Serious Health HazardOngoing
Medical DeviceMarch 13, 2019· COVIDIEN LLC

Recalled Item: Covidien Endo Clinch II Auto Suture Grasper Recalled by COVIDIEN LLC Due to...

The Issue: Sterilization method used was not consistent with the labeling and the...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 13, 2019· COVIDIEN LLC

Recalled Item: Covidien Endo Grasp Auto Suture Grasper 5mm The Recalled by COVIDIEN LLC Due...

The Issue: Sterilization method used was not consistent with the labeling and the...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 13, 2019· COVIDIEN LLC

Recalled Item: Procedure kits include devices from the affected lots distributed OUS...

The Issue: Sterilization method used was not consistent with the labeling and the...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 13, 2019· Exactech, Inc.

Recalled Item: Truliant Tibial Fit Tray Cemented SZ 3F / 3T Recalled by Exactech, Inc. Due...

The Issue: 2.5 Truliant Fit Trays were mismarked as 3

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

Class II — Potential Health HazardOngoing
DrugMarch 12, 2019· MSM Nutraceuticals, LLC

Recalled Item: Red Eye Recalled by MSM Nutraceuticals, LLC Due to Lack of Assurance of...

The Issue: Lack of Assurance of Sterility: Product is not terminally sterialized and...

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

Class II — Potential Health HazardOngoing
Refund
DrugMarch 12, 2019· MSM Nutraceuticals, LLC

Recalled Item: Dry Eye Recalled by MSM Nutraceuticals, LLC Due to Lack of Assurance of...

The Issue: Lack of Assurance of Sterility: Product is not terminally sterialized and...

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

Class II — Potential Health HazardOngoing
Refund