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. 2,386 recalls have been distributed to South Dakota in the last 12 months.

47,632 total recalls
2,386 in last 12 months

Showing 1990119920 of 47,632 recalls

Medical DeviceSeptember 17, 2019· Cook Inc.

Recalled Item: Pneumothorax Tray Recalled by Cook Inc. Due to Lidstock perforation line may...

The Issue: Lidstock perforation line may be over the sterile area of the tray, when it...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 16, 2019· Icecure Medical Ltd

Recalled Item: IceCure Cryoablation System ProSense -Intended for cryogenic destruction of...

The Issue: Updated User Manual DSR3200000 Rev. E to include the safety guidelines in...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 16, 2019· KT Health, LLC

Recalled Item: KT RECOVERY+ ICE/HEAT MASSAGE BALL Rolling ball with hot and Recalled by KT...

The Issue: If over-heated may leak which, if not noticed, may cause hot fluid to come...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 16, 2019· Medicrea International

Recalled Item: Medicrea Pass LP Trocar K-wire 01.6mm x 500mm-Nitinol Product Recalled by...

The Issue: Conical Cannulated Screws may not accept 1.6mm K-Wire, it cannot enter the...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 16, 2019· Medicrea International

Recalled Item: Medicrea Pass LP Blunt K-wire 01.6mm x 500mm-Nitinol Product : Recalled by...

The Issue: Conical Cannulated Screws may not accept 1.6mm K-Wire, it cannot enter the...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 16, 2019· Axis-Shield Diagnostics, Ltd.

Recalled Item: Axis-Shield Liquid Stable (LS) 2-Part HOMOCYSTEINE REAGENT Recalled by...

The Issue: There is a potential performance issue as detected by an under-recovery of...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 16, 2019· Axis-Shield Diagnostics, Ltd.

Recalled Item: Axis-Shield Liquid Stable (LS) 2-Part HOMOCYSTEINE REAGENT Recalled by...

The Issue: There is a potential performance issue as detected by an under-recovery of...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 16, 2019· Axis-Shield Diagnostics, Ltd.

Recalled Item: Axis-Shield Liquid Stable (LS) 2-Part HOMOCYSTEINE REAGENT Recalled by...

The Issue: There is a potential performance issue as detected by an under-recovery of...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 16, 2019· Abbott Gmbh & Co. KG

Recalled Item: Accessory kit Recalled by Abbott Gmbh & Co. KG Due to Potential reliability...

The Issue: Potential reliability issue with the Alinity ci series Level Sensor, Bulk...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 16, 2019· Abbott Gmbh & Co. KG

Recalled Item: Alinity ci Level Sensor Recalled by Abbott Gmbh & Co. KG Due to Potential...

The Issue: Potential reliability issue with the Alinity ci series Level Sensor, Bulk...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 16, 2019· Abbott Gmbh & Co. KG

Recalled Item: Accessory kit Recalled by Abbott Gmbh & Co. KG Due to Potential reliability...

The Issue: Potential reliability issue with the Alinity ci series Level Sensor, Bulk...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 16, 2019· GE Healthcare, LLC

Recalled Item: CardioLab/ComboLab Recording Systems Recalled by GE Healthcare, LLC Due to...

The Issue: Potential for failure of the patient leakage current test. There is a...

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

Class II — Potential Health HazardOngoing
DrugSeptember 13, 2019· GUERBET LLC

Recalled Item: Sodium Chloride Injection USP 0.9% Recalled by GUERBET LLC Due to Labeling:...

The Issue: Labeling: Not Elsewhere Classified: RFID formatting error which reads...

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

Class III — Low RiskOngoing
Refund
DrugSeptember 13, 2019· GUERBET LLC

Recalled Item: Optiray 320 (ioversol) Injection 68% Recalled by GUERBET LLC Due to...

The Issue: Labeling: Not Elsewhere Classified: RFID formatting error which reads...

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

Class II — Potential Health HazardOngoing
Refund
FoodSeptember 13, 2019· Abbott Laboratories

Recalled Item: Abbott Calcilo XD Recalled by Abbott Laboratories Due to Off color and odor....

The Issue: Off color and odor. Compromised can seam due to product (powder) in the...

Recommended Action: Do not consume. Return to store for a refund or discard.

Class II — Potential Health HazardOngoing
Refund
Medical DeviceSeptember 13, 2019· Draegar Medical Systems, Inc.

Recalled Item: The Infinity Acute Care System (IACS) Monitoring Solution with the Recalled...

The Issue: Cybersecurity vulnerabilities may cause device to reboot, lose alarm...

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

Class II — Potential Health HazardOngoing
DrugSeptember 12, 2019· KRS Global Biotechnology, Inc

Recalled Item: Sermorelin Recalled by KRS Global Biotechnology, Inc Due to Lack of...

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
DrugSeptember 12, 2019· KRS Global Biotechnology, Inc

Recalled Item: GLYCOpyrrolate (PF) 0.6 mg/3 mL (0.2 mg/mL) in 3 mL Single Dose Syringe...

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
DrugSeptember 12, 2019· KRS Global Biotechnology, Inc

Recalled Item: NEOstigmine Methylsulfate (PF) Recalled by KRS Global Biotechnology, Inc Due...

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
DrugSeptember 12, 2019· KRS Global Biotechnology, Inc

Recalled Item: Quadmix # 19 (Prostaglandin E1-0.75 mg / Papaverine HCl-150 mg 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