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 2604126060 of 47,632 recalls

DrugDecember 27, 2017· Pharmedium Services, LLC

Recalled Item: Ketamine HCl in 0.9% Sodium Chloride in all strengths Recalled by Pharmedium...

The Issue: Lack of sterility assurance.

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

Class II — Potential Health HazardOngoing
Refund
DrugDecember 27, 2017· Pharmedium Services, LLC

Recalled Item: Ketamine HCl Injection in all strengths Recalled by Pharmedium Services, LLC...

The Issue: Lack of sterility assurance.

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

Class II — Potential Health HazardOngoing
Refund
DrugDecember 27, 2017· Pharmedium Services, LLC

Recalled Item: Potassium Chloride in 0.9% Sodium Chloride in all strengths Recalled by...

The Issue: Lack of sterility assurance.

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

Class II — Potential Health HazardOngoing
Refund
Medical DeviceDecember 27, 2017· Ormco/Sybronendo

Recalled Item: Elements Obturation Unit (EOU) used with respective Buchanan Heat Pluggers...

The Issue: Buchanan Heat Pluggers will possibly overheat while used with the Elements...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 27, 2017· LITTLE RAPIDS CORPORATION

Recalled Item: EMS products from Graham Medical Recalled by LITTLE RAPIDS CORPORATION Due...

The Issue: The secondary supplier provided material was within specification but did...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 27, 2017· Mako Surgical Corporation

Recalled Item: Makoplasty RIO Standard System Recalled by Mako Surgical Corporation Due to...

The Issue: Communication-connection error.

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 22, 2017· DePuy Mitek, Inc., a Johnson & Johnson Co.

Recalled Item: LATARJET EXPERIENCE Sharp Curved Ostetome Product Usage: The Latarjet...

The Issue: Reports of product loosening or coming unscrewed from the handle.

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

Class II — Potential Health HazardOngoing
FoodDecember 22, 2017· Coconuthead, LLC

Recalled Item: CO YO Coconut Yogurt Alternative CHOCOLATE Recalled by Coconuthead, LLC Due...

The Issue: Coconuthead LLC is recalling CO YO Coconut Yogurt Alternative CHOCOLATE due...

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

Class II — Potential Health HazardOngoing
Refund
FoodDecember 22, 2017· Nodine's Smokehouse Inc.

Recalled Item: Smoked salmon in 1.5 oz. and 8 oz. packages Recalled by Nodine's Smokehouse...

The Issue: Product may be contaminated with Listeria monocytogenes.

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

Class I — Serious Health HazardOngoing
Refund
DrugDecember 22, 2017· Hetero Labs Limited Unit V

Recalled Item: Famciclovir Tablets Recalled by Hetero Labs Limited Unit V Due to...

The Issue: Temperature Abuse: Complaints of tablets being wet and stuck together with...

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

Class II — Potential Health HazardOngoing
Refund
DrugDecember 22, 2017· Hetero Labs, Ltd. - Unit III

Recalled Item: Simvastatin Tablets Recalled by Hetero Labs, Ltd. - Unit III Due to Presence...

The Issue: Presence of foreign substance: metallic razor blade was found in one bottle.

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

Class III — Low RiskOngoing
Refund
DrugDecember 21, 2017· Taro Pharmaceuticals U.S.A., Inc.

Recalled Item: Clobetasol Propionate Cream USP Recalled by Taro Pharmaceuticals U.S.A.,...

The Issue: Failed Content Uniformity Specifications

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

Class III — Low RiskOngoing
Refund
FoodDecember 21, 2017· Nutricia North America

Recalled Item: SHS Wel-Plan Wheat and Corn Strach Baking Mix Recalled by Nutricia North...

The Issue: Nutricia North America, Inc. has decided to recall SHS Wel-Plan Baking Mix ,...

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

Class II — Potential Health HazardOngoing
Refund
Medical DeviceDecember 21, 2017· DePuy Orthopaedics, Inc.

Recalled Item: (1) Sigma HP Cemented Trochlea Size 1 Narrow Left Recalled by DePuy...

The Issue: The SIGMA¿ HP PFJ Cemented Trochlear Implants, a standalone component of the...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 21, 2017· W & H DentalWerk Burmoos GMBH - Site 1

Recalled Item: Foot Controls Model: S-N1 and S-N2 Product Usage: Variable foot Recalled by...

The Issue: During continuous postmarket surveillance activities, we have noticed a...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 20, 2017· Integra LifeSciences Corp.

Recalled Item: The humeral stems trials are packaged in a kit for Recalled by Integra...

The Issue: Incidents of stem trial breakage were reported to the firm suggesting that...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 20, 2017· Ad-Tech Medical Instrument Corporation

Recalled Item: Disposable Drill Kit which includes two drill bits Recalled by Ad-Tech...

The Issue: There is a possibility that DDK2-2.4-30X Disposable Drill Kits, Lot Number...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 20, 2017· Merit Medical Systems, Inc.

Recalled Item: Flex-Neck Classic Peritoneal Dialysis Catheter (Pediatric) Product Usage: If...

The Issue: Mix-up between adult and pediatrics PD catheter.

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 20, 2017· Zimmer Biomet, Inc.

Recalled Item: ACE Trochanteric Nail System STER TROC END CAP STER TROC Recalled by Zimmer...

The Issue: Zimmer Biomet is conducting a medical device recall for the ACE Trochanteric...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 20, 2017· Zimmer Biomet, Inc.

Recalled Item: ACE Trochanteric Nail System STER L H TROC NAIL 320X9X125 Recalled by Zimmer...

The Issue: Zimmer Biomet is conducting a medical device recall for the ACE Trochanteric...

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

Class II — Potential Health HazardOngoing