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. 2,396 recalls have been distributed to South Dakota in the last 12 months.

47,632 total recalls
2,396 in last 12 months

Showing 1982119840 of 27,558 recalls

Medical DeviceMarch 31, 2016· American Surgical Company

Recalled Item: American Surgical Cotton Balls-Non-Strung 1/8" : 31-07 Product Usage:...

The Issue: Product packaging defective compromising sterility

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 31, 2016· American Surgical Company

Recalled Item: American Surgical Cotton Balls-Strung 3/8" : 30-01 Product Usage: Recalled...

The Issue: Product packaging defective compromising sterility

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 31, 2016· American Surgical Company

Recalled Item: American Surgical Ultracot 15 mm x 20 mm : Recalled by American Surgical...

The Issue: Product packaging defective compromising sterility

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 31, 2016· American Surgical Company

Recalled Item: American Surgical Americot Blue 3/8" x 3/8" : 20-22S Recalled by American...

The Issue: Product packaging defective compromising sterility

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 31, 2016· American Surgical Company

Recalled Item: American Surgical Americot Blue 1/2" x 3" : 20-07S Recalled by American...

The Issue: Product packaging defective compromising sterility

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 31, 2016· American Surgical Company

Recalled Item: American Surgical Americot Blue 1/2" x 1" : 20-05S Recalled by American...

The Issue: Product packaging defective compromising sterility

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 31, 2016· American Surgical Company

Recalled Item: American Surgical Ray-Cot 1" x 1" : 60-12 Product Recalled by American...

The Issue: Product packaging defective compromising sterility

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 31, 2016· American Surgical Company

Recalled Item: American Surgical Delicot 4 mm x 50 mm : Recalled by American Surgical...

The Issue: Product packaging defective compromising sterility

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 31, 2016· American Surgical Company

Recalled Item: American Surgical Ultracot 30 mm x 70 mm (Glassine) by American Surgical...

The Issue: Product packaging defective compromising sterility

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 31, 2016· American Surgical Company

Recalled Item: American Surgical Uniqcot 1/2" x 3" : 67-09 Product Recalled by American...

The Issue: Product packaging defective compromising sterility

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 31, 2016· American Surgical Company

Recalled Item: American Surgical Tonsil Sponges 1" Large : 50-01 Product Recalled by...

The Issue: Product packaging defective compromising sterility

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 31, 2016· American Surgical Company

Recalled Item: Mass Eye & Ear Finger Cot Nasal 2's : Recalled by American Surgical Company...

The Issue: Product packaging defective compromising sterility

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 31, 2016· St Jude Medical Inc.

Recalled Item: Ellipse ICD (Implantable Cardioverter Defibrillator) Model CD2411-36Q...

The Issue: St. Jude Medical is recalling the Ellipse ICD (Implantable Cardioverter...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 31, 2016· Shimadzu Medical Systems

Recalled Item: X-Ray Diagnostic Table Recalled by Shimadzu Medical Systems Due to Report of...

The Issue: Report of unintentional movement of table to reverse tilting.

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 31, 2016· Biocare Medical, LLC

Recalled Item: Mach 4 Mouse Probe vial within the Mach 4 Universal HRP-Polymer Kit Recalled...

The Issue: Biocare Medical has identified a single lot (082715) of its Mach 4 HRP...

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

Class III — Low RiskOngoing
Medical DeviceMarch 31, 2016· Siemens Medical Solutions USA, Inc.

Recalled Item: E.cam or Symbia systems that use foresight detectors - Product Recalled by...

The Issue: E. CAM and Symbia system with foresight detectors performing gated or...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 30, 2016· Teleflex Medical

Recalled Item: Pleur-evac Chest Drainage System Recalled by Teleflex Medical Due to The...

The Issue: The label on the Tyvek bag is missing. This is used by customers to identify...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 30, 2016· Siemens Healthcare Diagnostics, Inc.

Recalled Item: ADVIA Centaur CP Immunoassay System Recalled by Siemens Healthcare...

The Issue: The firm identified an issue in sample processing when using EZee-Nest...

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

Class III — Low RiskOngoing
Medical DeviceMarch 29, 2016· ev3, Inc.

Recalled Item: ev3 Recalled by ev3, Inc. Due to Mislabeling

The Issue: Medtronic is conducting a voluntary Urgent Medical Device Recall of two lots...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 28, 2016· Merge Healthcare, Inc.

Recalled Item: Merge Eye Station Import Utility (ESIU) when used with Merge Recalled by...

The Issue: Eye Station images were not importing properly and were imported under...

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

Class II — Potential Health HazardOngoing