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. 2,491 recalls have been distributed to South Dakota in the last 12 months.

47,632 total recalls
2,491 in last 12 months

Showing 1124111260 of 27,558 recalls

Medical DeviceJuly 8, 2020· Flower Orthopedics Corporation

Recalled Item: Calcaneus Plate Recalled by Flower Orthopedics Corporation Due to The...

The Issue: The contract manufacturer of the calcaneus plate inadvertently used the...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 8, 2020· Flower Orthopedics Corporation

Recalled Item: Calcaneus Plate Recalled by Flower Orthopedics Corporation Due to The...

The Issue: The contract manufacturer of the calcaneus plate inadvertently used the...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 8, 2020· Flower Orthopedics Corporation

Recalled Item: Calcaneus Plate Recalled by Flower Orthopedics Corporation Due to The...

The Issue: The contract manufacturer of the calcaneus plate inadvertently used the...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 8, 2020· Flower Orthopedics Corporation

Recalled Item: Calcaneus Plate Recalled by Flower Orthopedics Corporation Due to The...

The Issue: The contract manufacturer of the calcaneus plate inadvertently used the...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 8, 2020· Flower Orthopedics Corporation

Recalled Item: Calcaneus Plate Recalled by Flower Orthopedics Corporation Due to The...

The Issue: The contract manufacturer of the calcaneus plate inadvertently used the...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 8, 2020· Flower Orthopedics Corporation

Recalled Item: Calcaneus Plate Recalled by Flower Orthopedics Corporation Due to The...

The Issue: The contract manufacturer of the calcaneus plate inadvertently used the...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 8, 2020· New Wave Endo-Surgical, Corp.

Recalled Item: M-Close Kit Recalled by New Wave Endo-Surgical, Corp. Due to The plastic...

The Issue: The plastic housing on the device may fracture

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 6, 2020· ICU Medical, Inc.

Recalled Item: 54 IN (137 cm) APPX 7.2 ml EXT SET w NanoClave 4-Way Stopcock Recalled by...

The Issue: Identification of a potential manufacturing defect on the internal surface...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 6, 2020· ICU Medical, Inc.

Recalled Item: APPX 0.75ml Recalled by ICU Medical, Inc. Due to Identification of a...

The Issue: Identification of a potential manufacturing defect on the internal surface...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 6, 2020· ICU Medical, Inc.

Recalled Item: 126" (320 cm) 16.4 ml Recalled by ICU Medical, Inc. Due to Identification of...

The Issue: Identification of a potential manufacturing defect on the internal surface...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 6, 2020· ICU Medical, Inc.

Recalled Item: 7" (18 cm) Appx 0.29 ml Recalled by ICU Medical, Inc. Due to Identification...

The Issue: Identification of a potential manufacturing defect on the internal surface...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 6, 2020· ICU Medical, Inc.

Recalled Item: 112" (284 cm) 60 Drop 150ml Burette Set (Clave Recalled by ICU Medical, Inc....

The Issue: Identification of a potential manufacturing defect on the internal surface...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 6, 2020· ICU Medical, Inc.

Recalled Item: 7 IN (18CM) APPX 0.26ml Recalled by ICU Medical, Inc. Due to Identification...

The Issue: Identification of a potential manufacturing defect on the internal surface...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 6, 2020· ICU Medical, Inc.

Recalled Item: Appx 0.82 ml Recalled by ICU Medical, Inc. Due to Identification of a...

The Issue: Identification of a potential manufacturing defect on the internal surface...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 6, 2020· ICU Medical, Inc.

Recalled Item: 83" (211 cm) Smallbore Ext Set w/Remv 8 Gang 4-Way Recalled by ICU Medical,...

The Issue: Identification of a potential manufacturing defect on the internal surface...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 6, 2020· ICU Medical, Inc.

Recalled Item: 13 IN (33cm) APPX 0.96 ml Recalled by ICU Medical, Inc. Due to...

The Issue: Identification of a potential manufacturing defect on the internal surface...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 6, 2020· ICU Medical, Inc.

Recalled Item: 13 IN(33cm) APPX 1.0 ml Recalled by ICU Medical, Inc. Due to Identification...

The Issue: Identification of a potential manufacturing defect on the internal surface...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 6, 2020· ICU Medical, Inc.

Recalled Item: 7" (18cm) Appx 0.31 ml Recalled by ICU Medical, Inc. Due to Identification...

The Issue: Identification of a potential manufacturing defect on the internal surface...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 6, 2020· ICU Medical, Inc.

Recalled Item: 6.5" (17 cm) Appx 0.35 ml Recalled by ICU Medical, Inc. Due to...

The Issue: Identification of a potential manufacturing defect on the internal surface...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 6, 2020· ICU Medical, Inc.

Recalled Item: 114" (290 cm) 60 Drop 150ml Burette Set (Clave Recalled by ICU Medical, Inc....

The Issue: Identification of a potential manufacturing defect on the internal surface...

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

Class II — Potential Health HazardOngoing