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. 2,512 recalls have been distributed to South Dakota in the last 12 months.

47,632 total recalls
2,512 in last 12 months

Showing 96419660 of 47,632 recalls

Medical DeviceFebruary 13, 2023· Maquet Medical Systems USA

Recalled Item: BEQ-HLS 5050 USA Recalled by Maquet Medical Systems USA Due to Firm has...

The Issue: Firm has initiated a removal of the product due to insufficient evidence of...

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

Class II — Potential Health HazardOngoing
DrugFebruary 10, 2023· B. Braun Medical Inc.

Recalled Item: 0.9% Sodium Chloride Injection Recalled by B. Braun Medical Inc. Due to Lack...

The Issue: Lack of sterility assurance: Recall of certain batches of 0.9% Sodium...

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

Class II — Potential Health HazardOngoing
Refund
DrugFebruary 10, 2023· B. Braun Medical Inc.

Recalled Item: 0.9% Sodium Chloride Injection Recalled by B. Braun Medical Inc. Due to Lack...

The Issue: Lack of sterility assurance: Recall of certain batches of 0.9% Sodium...

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

Class II — Potential Health HazardOngoing
Refund
Medical DeviceFebruary 10, 2023· Philips Respironics, Inc.

Recalled Item: Philips DreamStation Auto BiPAP and CPAP Recalled by Philips Respironics,...

The Issue: A limited number of remediated Philips DreamStation units may experience...

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

Class I — Serious Health HazardOngoing
Medical DeviceFebruary 10, 2023· Unetixs Vascular, Inc.

Recalled Item: MultiLab Series II ROODRA non-invasive vascular diagnostic device Recalled...

The Issue: The current luer fittings and adaptors allow for the possibility of the air...

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 10, 2023· Unetixs Vascular, Inc.

Recalled Item: MultiLab Series II 2CP & 2CP Express non-invasive vascular diagnostic device...

The Issue: The current luer fittings and adaptors allow for the possibility of the air...

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 10, 2023· Unetixs Vascular, Inc.

Recalled Item: MultiLab Series II REVO non-invasive vascular diagnostic device Recalled by...

The Issue: The current luer fittings and adaptors allow for the possibility of the air...

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 10, 2023· Unetixs Vascular, Inc.

Recalled Item: MultiLab Series II LHS TI & ERGO non-invasive vascular diagnostic device...

The Issue: The current luer fittings and adaptors allow for the possibility of the air...

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

Class II — Potential Health HazardOngoing
DrugFebruary 9, 2023· L. Perrigo Company

Recalled Item: allergy relief Recalled by L. Perrigo Company Due to Failed...

The Issue: Failed Impurities/Degradation Specifications

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

Class II — Potential Health HazardOngoing
Refund
DrugFebruary 9, 2023· L. Perrigo Company

Recalled Item: Allergy Relief Recalled by L. Perrigo Company Due to Failed...

The Issue: Failed Impurities/Degradation Specifications

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

Class II — Potential Health HazardOngoing
Refund
DrugFebruary 9, 2023· L. Perrigo Company

Recalled Item: allergyrelief Recalled by L. Perrigo Company Due to Failed...

The Issue: Failed Impurities/Degradation Specifications

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

Class II — Potential Health HazardOngoing
Refund
DrugFebruary 9, 2023· L. Perrigo Company

Recalled Item: allergy relief Recalled by L. Perrigo Company Due to Failed...

The Issue: Failed Impurities/Degradation Specifications

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

Class II — Potential Health HazardOngoing
Refund
DrugFebruary 9, 2023· L. Perrigo Company

Recalled Item: Allergy Relief Recalled by L. Perrigo Company Due to Failed...

The Issue: Failed Impurities/Degradation Specifications

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

Class II — Potential Health HazardOngoing
Refund
DrugFebruary 9, 2023· L. Perrigo Company

Recalled Item: Fexofenadine Hydrochloride Tablets Recalled by L. Perrigo Company Due to...

The Issue: Failed Impurities/Degradation Specifications

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

Class II — Potential Health HazardOngoing
Refund
DrugFebruary 9, 2023· L. Perrigo Company

Recalled Item: Allergy Relief Recalled by L. Perrigo Company Due to Failed...

The Issue: Failed Impurities/Degradation Specifications

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

Class II — Potential Health HazardOngoing
Refund
DrugFebruary 9, 2023· L. Perrigo Company

Recalled Item: Fexofenadine Hydrochloride Tablets Recalled by L. Perrigo Company Due to...

The Issue: Failed Impurities/Degradation Specifications

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

Class II — Potential Health HazardOngoing
Refund
DrugFebruary 9, 2023· L. Perrigo Company

Recalled Item: Picnic Recalled by L. Perrigo Company Due to Failed Impurities/Degradation...

The Issue: Failed Impurities/Degradation Specifications

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

Class II — Potential Health HazardOngoing
Refund
DrugFebruary 9, 2023· L. Perrigo Company

Recalled Item: Allergy Recalled by L. Perrigo Company Due to Failed Impurities/Degradation...

The Issue: Failed Impurities/Degradation Specifications

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

Class II — Potential Health HazardOngoing
Refund
DrugFebruary 9, 2023· L. Perrigo Company

Recalled Item: Non-Drowsy Allergy Relief Recalled by L. Perrigo Company Due to Failed...

The Issue: Failed Impurities/Degradation Specifications

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

Class II — Potential Health HazardOngoing
Refund
DrugFebruary 9, 2023· L. Perrigo Company

Recalled Item: Allergy ALLER-FEX Recalled by L. Perrigo Company Due to Failed...

The Issue: Failed Impurities/Degradation Specifications

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

Class II — Potential Health HazardOngoing
Refund