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 1986119880 of 27,558 recalls

Medical DeviceMarch 23, 2016· Acumedia Manufacturers, Inc.

Recalled Item: Nutrient Gelatin Recalled by Acumedia Manufacturers, Inc. Due to Incorrect...

The Issue: Incorrect expiration date was listed on the label. Correct expiration date...

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

Class III — Low RiskOngoing
Medical DeviceMarch 22, 2016· Coloplast Manufacturing US, LLC

Recalled Item: Self-Cath¿ Pediatric Catheter Size CH 06 Recalled by Coloplast Manufacturing...

The Issue: Coloplast Corp. is voluntarily recalling a single lot of Self-Cath Pediatric...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 22, 2016· Boston Scientific Corporation

Recalled Item: Boston Scientific Fetch 2 Aspiration Catheter Recalled by Boston Scientific...

The Issue: Boston Scientific is recalling all models of Fetch 2 Aspiration Catheter as...

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

Class I — Serious Health HazardOngoing
Medical DeviceMarch 22, 2016· Medscience Inc

Recalled Item: AllergiEnd ST-9 Multiple Skin Test Applicator (Item 1000) and AllergiEnd...

The Issue: During an FDA inspection it was found that the products are marketed without...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 21, 2016· Windstone Medical Packaging, Inc.

Recalled Item: General Surgery Pack Recalled by Windstone Medical Packaging, Inc. Due to...

The Issue: These packs contain item #4037 Kerlix X-ray Detectable Laparotomy Sponges...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 21, 2016· Stryker Neurovascular

Recalled Item: GDC-10 360 SOFT 10MM X 20CM SR Detachable Coil Sterile Recalled by Stryker...

The Issue: The incorrect DFU was packaged with two lots of GDC 360 degree Detachable Coils.

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 21, 2016· Windstone Medical Packaging, Inc.

Recalled Item: Laparotomy Pack Latex Free Recalled by Windstone Medical Packaging, Inc. Due...

The Issue: These packs contain item #4037 Kerlix X-ray Detectable Laparotomy Sponges...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 21, 2016· Stryker Neurovascular

Recalled Item: GDC-18 360 11MM X 30CM Detachable Coil Sterile Recalled by Stryker...

The Issue: The incorrect DFU was packaged with two lots of GDC 360 degree Detachable Coils.

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 21, 2016· Windstone Medical Packaging, Inc.

Recalled Item: Laparotomy Pack Recalled by Windstone Medical Packaging, Inc. Due to These...

The Issue: These packs contain item #4037 Kerlix X-ray Detectable Laparotomy Sponges...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 21, 2016· Angiodynamics Inc. (Navilyst Medical Inc.)

Recalled Item: Vortex MEDICAL AngioVac Circuit Recalled by Angiodynamics Inc. (Navilyst...

The Issue: Maquet Cardiopulmonary, the manufacturer of the RotaFlow Centrifugal Pump,...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 21, 2016· Angiodynamics Inc. (Navilyst Medical Inc.)

Recalled Item: AngioVac Circuit Pack (Tandem Packs) Recalled by Angiodynamics Inc....

The Issue: Maquet Cardiopulmonary, the manufacturer of the RotaFlow Centrifugal Pump,...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 21, 2016· Stryker Instruments Div. of Stryker Corporation

Recalled Item: SurgiCounter scanner Recalled by Stryker Instruments Div. of Stryker...

The Issue: The affected scanner does not correctly interact with the SC360 software....

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 18, 2016· Boston Scientific Corporation

Recalled Item: Boston Scientific Ultraflex Tracheobronchial Distal Release Stent System...

The Issue: Mislabeled: 10mm diameter x 30mm length Ultraflex Tracheobronchial stents...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 18, 2016· Becton Dickinson & Company

Recalled Item: 1) 24 G x 0.75 in. BD Angiocath" Autoguard" shielded Recalled by Becton...

The Issue: The device may have a defect in the catheter. In some instances this defect...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 17, 2016· Siemens Healthcare Diagnostics, Inc.

Recalled Item: Dimension Assays: Direct HDL Cholesterol (AHDL) Recalled by Siemens...

The Issue: Siemens Healthcare Diagnostics has become aware of N-Acetylcysteine (NAC)...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 17, 2016· Siemens Healthcare Diagnostics, Inc.

Recalled Item: Dimension Vista Assays: Triglycerides (TRIG) Recalled by Siemens Healthcare...

The Issue: Siemens Healthcare Diagnostics has become aware of N-Acetylcysteine (NAC)...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 17, 2016· Siemens Healthcare Diagnostics, Inc.

Recalled Item: ADVIA CHEMISTRY TRIGLYCERIDES_2 (TRIG_2) REAGENT & ADVIA CHEMISTRY...

The Issue: Siemens Healthcare Diagnostics has become aware of N-Acetylcysteine (NAC)...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 17, 2016· Siemens Healthcare Diagnostics, Inc.

Recalled Item: Dimension Vista Assays: Direct HDL Cholesterol (AHDL) Recalled by Siemens...

The Issue: Siemens Healthcare Diagnostics has become aware of N-Acetylcysteine (NAC)...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 17, 2016· Medtronic Navigation, Inc.-Littleton

Recalled Item: Medtronic 0-arm Imaging mobile x-ray system. Model Numbers - B1-700-00027...

The Issue: It has been discovered that replacement x-ray generator and system motion...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 17, 2016· Siemens Healthcare Diagnostics, Inc.

Recalled Item: Dimension Vista Assays: Uric Acid (URCA) Recalled by Siemens Healthcare...

The Issue: Siemens Healthcare Diagnostics has become aware of N-Acetylcysteine (NAC)...

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

Class II — Potential Health HazardOngoing