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. 1,670 recalls have been distributed to South Dakota in the last 12 months.

47,632 total recalls
1,670 in last 12 months

Showing 4164141660 of 47,632 recalls

Medical DeviceNovember 4, 2013· Stryker Neurovascular

Recalled Item: Stryker brand EXCELSIOR SL-10 PRE-SHAPED S 15OCM Recalled by Stryker...

The Issue: Products were shipped labeled with "use by" dates that exceed currently...

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

Class II — Potential Health HazardOngoing
DrugNovember 4, 2013· Greenstone Llc

Recalled Item: Glipizide XL (glipizide) extended release tablets Recalled by Greenstone Llc...

The Issue: Failed Dissolution Specification; the bulk lot yielded an out of...

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

Class III — Low RiskOngoing
Refund
DrugNovember 4, 2013· Pfizer Inc.

Recalled Item: Glucotrol XL (glipizide) extended release tablets Recalled by Pfizer Inc....

The Issue: Failed Dissolution Specification; 8 hr stability timepoint

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

Class III — Low RiskOngoing
Refund
DrugNovember 4, 2013· Alexion Pharmaceuticals, Inc.

Recalled Item: Soliris (eculizumab) Concentrated Solution for Intravenous Infusion Only...

The Issue: Presence of Particulate Matter: Failed the appearance test for the presence...

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

Class I — Serious Health HazardOngoing
Refund
DrugNovember 4, 2013· IQ Formulations, LLC

Recalled Item: Hydravax High Potency Diuretic Weight Loss Solution Recalled by IQ...

The Issue: Marketed Without an Approved NDA/ANDA; this product is being recalled for...

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

Class I — Serious Health HazardOngoing
Refund
DrugNovember 1, 2013· L. Perrigo Co.

Recalled Item: Acetaminophen suspension liquid Recalled by L. Perrigo Co. Due to Defective...

The Issue: Defective Delivery System: There is a remote potential that cartons of...

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

Class II — Potential Health HazardOngoing
Refund
DrugNovember 1, 2013· L. Perrigo Co.

Recalled Item: Acetaminophen suspension liquid Recalled by L. Perrigo Co. Due to Defective...

The Issue: Defective Delivery System: There is a remote potential that cartons of...

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

Class II — Potential Health HazardOngoing
Refund
DrugNovember 1, 2013· Greenstone Llc

Recalled Item: Nifedipine Recalled by Greenstone Llc Due to Labeling: Incorrect or Missing...

The Issue: Labeling: Incorrect or Missing Lot and/or Exp Date: Greenstone LLC is...

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

Class II — Potential Health HazardOngoing
Refund
DrugNovember 1, 2013· Sigma-Tau Pharmaceuticals, Inc.

Recalled Item: PEGASPARGASE ONCASPAR Injection Recalled by Sigma-Tau Pharmaceuticals, Inc....

The Issue: Lack of Assurance of Sterility: Sigma-Tau PharmaSource, Inc. is conducting a...

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

Class II — Potential Health HazardOngoing
Refund
DrugNovember 1, 2013· L. Perrigo Co.

Recalled Item: Acetaminophen suspension liquid Recalled by L. Perrigo Co. Due to Defective...

The Issue: Defective Delivery System: There is a remote potential that cartons of...

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

Class II — Potential Health HazardOngoing
Refund
DrugNovember 1, 2013· L. Perrigo Co.

Recalled Item: Acetaminophen suspension liquid Recalled by L. Perrigo Co. Due to Defective...

The Issue: Defective Delivery System: There is a remote potential that cartons of...

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

Class II — Potential Health HazardOngoing
Refund
Medical DeviceNovember 1, 2013· Stryker Instruments Div. of Stryker Corporation

Recalled Item: Acetabular Pressurizer Recalled by Stryker Instruments Div. of Stryker...

The Issue: On March 14, 2013 a Work Order was opened for 120 units (20 boxes) of the...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 31, 2013· Hospira Inc.

Recalled Item: Abbott Acclaim Infusion Pump Designed to deliver parenteral infusions...

The Issue: Hospira has received customer reports of broken door assemblies on the...

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

Class I — Serious Health HazardOngoing
Medical DeviceOctober 31, 2013· Hospira Inc.

Recalled Item: Hospira Acclaim Encore Infusion Pump Designed to deliver parenteral...

The Issue: Broken door assemblies on the Hospira/Abbott Acclaim Encore infusion pumps....

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

Class I — Serious Health HazardOngoing
Medical DeviceOctober 31, 2013· Zimmer, Inc.

Recalled Item: NexGen¿ Complete Knee Solutions Stemmed Tibial Component Precoat NexGen...

The Issue: Two complaints were received in which it was reported that the stem would...

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

Class II — Potential Health HazardOngoing
DrugOctober 31, 2013· Fresenius Kabi USA, LLC

Recalled Item: Tranexamic Acid Injection USP Recalled by Fresenius Kabi USA, LLC Due to...

The Issue: Presence of Particulate Matter: Particulate matter consistent with...

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

Class II — Potential Health HazardOngoing
Refund
Medical DeviceOctober 30, 2013· Ergosafe Products LLC DBA Prism Medical Services USA

Recalled Item: Medcare Products Max-500 Stand-N-Weigh Recalled by Ergosafe Products LLC DBA...

The Issue: The lift might fail with the labeled 500-lb. load rating.

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 30, 2013· Ergosafe Products LLC DBA Prism Medical Services USA

Recalled Item: Medcare Products Max-500 Stand Recalled by Ergosafe Products LLC DBA Prism...

The Issue: The lift might fail with the labeled 500-lb. load rating.

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 30, 2013· Philips Medical Systems, Inc.

Recalled Item: Easy Diagnost Eleva Universal Fluoroscopic applications Recalled by Philips...

The Issue: The delivered application software was an outdated version to the model of...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 30, 2013· Maquet Cardiovascular, LLC

Recalled Item: Vasoview Hemopro Endoscopic Vessel Harvesting System Maquet Cardiovascular...

The Issue: Maquet has received an increase in the number of complaints for...

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

Class II — Potential Health HazardOngoing