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. 2,349 recalls have been distributed to South Dakota in the last 12 months.

47,632 total recalls
2,349 in last 12 months

Showing 2546125480 of 47,632 recalls

Medical DeviceMarch 21, 2018· Siemens Healthcare Diagnostics, Inc.

Recalled Item: Dimension Vista¿ MULTI 2 SDIL Recalled by Siemens Healthcare Diagnostics,...

The Issue: The diluent may have an incomplete slit on the septum in the cap of the...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 21, 2018· Siemens Healthcare Diagnostics, Inc.

Recalled Item: Dimension Vista¿ CTNI Sample Diluent Recalled by Siemens Healthcare...

The Issue: The diluent may have an incomplete slit on the septum in the cap of the...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 21, 2018· Siemens Healthcare Diagnostics, Inc.

Recalled Item: Dimension Vista¿ MULTI 1 SDIL Recalled by Siemens Healthcare Diagnostics,...

The Issue: The diluent may have an incomplete slit on the septum in the cap of the...

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

Class II — Potential Health HazardOngoing
DrugMarch 21, 2018· Mayne Pharma Inc

Recalled Item: Fabior (tazarotene) Foam Recalled by Mayne Pharma Inc Due to Superpotent...

The Issue: Superpotent Drug: High out of specification results for tazarotene assay at...

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

Class III — Low RiskOngoing
Refund
FoodMarch 21, 2018· Poppies International INC

Recalled Item: GFS Belgian Mini Chocolate Topped Eclairs Recalled by Poppies International...

The Issue: Products may be contaminated with Listeria monocytogenes

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

Class II — Potential Health HazardOngoing
Refund
FoodMarch 21, 2018· Swire Coca Cola USA

Recalled Item: Dr. Pepper Est. 1885 Diet Recalled by Swire Coca Cola USA Due to Foreign...

The Issue: Swire Coca Cola is recalling certain Diet Dr Pepper bottle due to the...

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

Class II — Potential Health HazardOngoing
Refund
FoodMarch 20, 2018· Pepsi Cola Bottling Company

Recalled Item: Diet Pepsi Recalled by Pepsi Cola Bottling Company Due to Case labeling...

The Issue: Case labeling (shrink-wrap labeling) for Diet Pepsi 6 packs (6-16oz bottles)...

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

Class III — Low RiskOngoing
Refund
Medical DeviceMarch 20, 2018· Becton Dickinson & Company

Recalled Item: BD Vacutainer¿ Push Button Blood Collection Set 0.8 x 19 Recalled by Becton...

The Issue: Products do not meet the labeled sterility claim of a Sterility Assurance...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 20, 2018· Becton Dickinson & Company

Recalled Item: BD Vacutainer¿ Ultra TouchTM Push Button Blood Collection Set 0.6 Recalled...

The Issue: Products do not meet the labeled sterility claim of a Sterility Assurance...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 20, 2018· Becton Dickinson & Company

Recalled Item: BD Vacutainer¿ Push Button Blood Collection Set 0.6 x 19 Recalled by Becton...

The Issue: Products do not meet the labeled sterility claim of a Sterility Assurance...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 20, 2018· Certified Safety Mfg Inc

Recalled Item: First aid/emergency kits containing Honeywell eyewash: CSM kit number...

The Issue: Firm is recalling first aid/emergency kits and cabinets which contain...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 19, 2018· Synthes, Inc.

Recalled Item: Stem Extractor f/Guide Bar Recalled by Synthes, Inc. Due to There is a...

The Issue: There is a potential for the connection screw of the stem extractor to break.

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

Class II — Potential Health HazardOngoing
DrugMarch 19, 2018· Glenmark Pharmaceuticals Inc., USA

Recalled Item: Indomethacin Capsules USP Recalled by Glenmark Pharmaceuticals Inc., USA Due...

The Issue: Labeling: Incorrect Instructions: bottles incorrectly labeled with the usual...

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

Class III — Low RiskOngoing
Refund
FoodMarch 16, 2018· NGB, Corp

Recalled Item: Nxtgen Botanicals Recalled by NGB, Corp Due to Potential Salmonella...

The Issue: NGB Corp is recalling Nxtgen Botanicals due to potential Salmonella...

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

Class I — Serious Health HazardOngoing
Refund
FoodMarch 16, 2018· Natural Grocers by Vitamin Cottage

Recalled Item: Natural Grocers Organic Coconut Smiles Recalled by Natural Grocers by...

The Issue: Coconut smiles product tested positive for Salmonella.

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

Class I — Serious Health HazardOngoing
Refund
Medical DeviceMarch 16, 2018· Nobel Biocare Usa Llc

Recalled Item: Nobel Biocare 17¿ Multi-Unit Abutment Recalled by Nobel Biocare Usa Llc Due...

The Issue: The product label has missing information, such as the lot number and...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 16, 2018· GE Medical Systems Ultrasound & Primary Care Diagnostics, LL

Recalled Item: GE Healthcare: a) Prodigy Recalled by GE Medical Systems Ultrasound &...

The Issue: Under certain conditions, when using DICOM Worklist along with DICOM MPPS, a...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 16, 2018· Philips Electronics North America Corporation

Recalled Item: Achieva 1.5T: 1) Nova (Dual) Recalled by Philips Electronics North America...

The Issue: Potential risk for helium gas inside the MR examination room during a magnet...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 16, 2018· Philips Electronics North America Corporation

Recalled Item: Conversion SmarthPath to dStream for 1.5T Recalled by Philips Electronics...

The Issue: Potential risk for helium gas inside the MR examination room during a magnet...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 16, 2018· GE Medical Systems Ultrasound & Primary Care Diagnostics, LL

Recalled Item: GE Healthcare Lunar: a) DPX NT Recalled by GE Medical Systems Ultrasound &...

The Issue: Under certain conditions, when using DICOM Worklist along with DICOM MPPS, a...

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

Class II — Potential Health HazardOngoing