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. 2,339 recalls have been distributed to South Dakota in the last 12 months.

47,632 total recalls
2,339 in last 12 months

Showing 3316133180 of 47,632 recalls

Medical DeviceMarch 3, 2016· Covidien LLC

Recalled Item: Curity X-Ray Detectable Laparotomy Sponges Recalled by Covidien LLC Due to...

The Issue: Compromised sterility due to breach of barrier

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 3, 2016· Covidien LLC

Recalled Item: Curity X-Ray Detectable Laparotomy Sponges Recalled by Covidien LLC Due to...

The Issue: Compromised sterility due to breach of barrier

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 3, 2016· Covidien LLC

Recalled Item: Curity X-Ray Detectable Laparotomy Sponges Recalled by Covidien LLC Due to...

The Issue: Compromised sterility due to breach of barrier

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 3, 2016· Roche Molecular Systems, Inc.

Recalled Item: Hand-Held Scanner USB IT3800 For sample identification and tracking when...

The Issue: The hand-held barcode scanner model IT3800 used with the COBAS AmpliPrep...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 3, 2016· Dynarex Corporation

Recalled Item: dynarex Specimen Containers Recalled by Dynarex Corporation Due to Exterior...

The Issue: Exterior carton is mis-labeled as Sterile. Non-sterile, bulk specimen...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 3, 2016· ArthroCare Corporation

Recalled Item: TOPAZ MicroDebrider 0.8 mm Recalled by ArthroCare Corporation Due to During...

The Issue: During functional testing of devices after real time aging, it was...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 3, 2016· Covidien LLC

Recalled Item: Kerlix" X-Ray Detectable Laparotomy Sponges Recalled by Covidien LLC Due to...

The Issue: Compromised sterility due to breach of barrier

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 3, 2016· Covidien LLC

Recalled Item: Curity X-Ray Detectable Laparotomy Sponges Recalled by Covidien LLC Due to...

The Issue: Compromised sterility due to breach of barrier

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 3, 2016· Covidien LLC

Recalled Item: Curity" X-Ray Detectable Laparotomy Sponges Recalled by Covidien LLC Due to...

The Issue: Compromised sterility due to breach of barrier

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 3, 2016· Covidien LLC

Recalled Item: Vistec X-Ray Detectable Sponges Recalled by Covidien LLC Due to Compromised...

The Issue: Compromised sterility due to breach of barrier

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 3, 2016· Covidien LLC

Recalled Item: Curity All Purpose Sponges Recalled by Covidien LLC Due to Compromised...

The Issue: Compromised sterility due to breach of barrier

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 3, 2016· Covidien LLC

Recalled Item: Kerlix X-Ray Detectable Laparotomy Sponges Recalled by Covidien LLC Due to...

The Issue: Compromised sterility due to breach of barrier

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

Class II — Potential Health HazardOngoing
FoodMarch 3, 2016· Hy-Vee Stores Inc

Recalled Item: Whole wheels and cuts of Maytag blue cheese re-packaged in Recalled by...

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
FoodMarch 3, 2016· Hy-Vee Stores Inc

Recalled Item: Maytag Blue cheese crumbles re-packaged and sold in plastic containers...

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
DrugMarch 3, 2016· Dr. Reddy's Laboratories, Inc.

Recalled Item: Zoledronic Acid Injection Recalled by Dr. Reddy's Laboratories, Inc. Due to...

The Issue: Lack of Assurance of Sterility; defective seals where the metal silver ring...

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

Class II — Potential Health HazardOngoing
Refund
Medical DeviceMarch 2, 2016· Siemens Medical Solutions USA, Inc

Recalled Item: Siemens SOMATOM Definition Flash Recalled by Siemens Medical Solutions USA,...

The Issue: Software bugs in these SOMATOM systems could possibly cause scan aborts,...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 2, 2016· Siemens Medical Solutions USA, Inc

Recalled Item: Siemens SOMATOM Definition: Intended to produce cross-sectional images of...

The Issue: Software bugs in these SOMATOM systems could possibly cause scan aborts,...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 2, 2016· Siemens Medical Solutions USA, Inc

Recalled Item: Siemens SOMATOM Definition Recalled by Siemens Medical Solutions USA, Inc...

The Issue: Software bugs in these SOMATOM systems could possibly cause scan aborts,...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 2, 2016· Siemens Medical Solutions USA, Inc

Recalled Item: Siemens SOMATOM Definition AS Recalled by Siemens Medical Solutions USA, Inc...

The Issue: Software bugs in these SOMATOM systems could possibly cause scan aborts,...

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

Class II — Potential Health HazardOngoing
FoodMarch 2, 2016· ProSupps USA LLC

Recalled Item: Prosupps Mr. Hyde INTENSE ENERGY PRE WORKOUT 15 SERVINGS BLUERAZZ Recalled...

The Issue: Product could be potentially mislabeled and contain non-dietary ingredient...

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

Class II — Potential Health HazardOngoing
Refund