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 16061–16080 of 47,632 recalls

Medical DeviceDecember 18, 2020· Siemens Medical Solutions USA, Inc

Recalled Item: ARTIS Icono biplane Model:11327600 ARTIS Icono floor system Model: 11327700...

The Issue: Misleading error messages and a gap in the Operator Manual which affects...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 18, 2020· Hill-Rom, Inc.

Recalled Item: Liko Multirall 200 overhead lift- overhead lift is a general-purpose...

The Issue: Multirall Q-link strap lock has not been fully engaged in the S65 rail...

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

Class I — Serious Health HazardOngoing
Medical DeviceDecember 18, 2020· Smith & Nephew, Inc.

Recalled Item: VERSABOND AB 40 GRAMS FORMULATION 2 Recalled by Smith & Nephew, Inc. Due to...

The Issue: Potential heat and humidity exposure. The affected lot contained an atypical...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 18, 2020· Alung Technologies Inc

Recalled Item: ALung Technologies Hemolung Respiratory Assist System (RAS) with CME...

The Issue: CME America BodyGuard 323 Infusion Pumps (recalled by manufacturer) is a...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 17, 2020· Fresenius Medical Care Holdings, Inc.

Recalled Item: Fresenius Medical Care NaturaLyte Liquid Acid concentrate-Liquid Acid...

The Issue: Bottles Missing Product Label

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 17, 2020· GE Healthcare, LLC

Recalled Item: System Recalled by GE Healthcare, LLC Due to GE Healthcare has become aware...

The Issue: GE Healthcare has become aware of a potential issue on Revolution Apex,...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 17, 2020· Roche Diagnostics Operations, Inc.

Recalled Item: A calculator/data processing module for clinical use is an electronic...

The Issue: A software error results in the unintentional removal of the serum-indices...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 17, 2020· Bioventus, LLC

Recalled Item: EXOGEN Ultrasound Coupling Gel Recalled by Bioventus, LLC Due to Product may...

The Issue: Product may contain white particulates that are microbial in nature.

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 17, 2020· GE Healthcare, LLC

Recalled Item: System Recalled by GE Healthcare, LLC Due to GE Healthcare has become aware...

The Issue: GE Healthcare has become aware of a potential issue on Revolution Apex,...

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

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

Recalled Item: ePHEDrine 25 mg/5 mL in 0.9% Sodium Chloride Injection Recalled by SCA...

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: Lidocaine HCl 2% 5 mL Recalled by SCA Pharmaceuticals Due to Lack of...

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 30 mg/30 mL in 0.9% Sodium Chloride (1mg/ml) 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: Ketamine 100 mg/10mL in 0.9% Sodium Chloride Injection (10 mg/mL) Recalled...

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: fentaNYL 1500 mcg/30 mL (50 mcg/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: HYDROmorphone HCl 30 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· SCA Pharmaceuticals

Recalled Item: fentaNYL 100 mcg/50mL Bupivacaine HCl 0.125% 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: Morphine Sulfate 3 mg/3 mL in 0.9% Sodium Chloride (1mg/mL) CII 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 III — Low RiskOngoing
Refund
DrugDecember 17, 2020· SCA Pharmaceuticals

Recalled Item: PHENYLephrine HCl 500 mcg/5mL in 0.9% Sodium Chloride (100 mcg/mL) Recalled...

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: labetalol HCl 20 mg/4 mL Recalled by SCA Pharmaceuticals Due to Lack of...

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 6 mg/30mL in 0.9% Sodium Chloride Injection (0.2 mg/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