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. 2,484 recalls have been distributed to South Dakota in the last 12 months.
Showing 13161–13180 of 47,632 recalls
Recalled Item: BD Vacutainer Luer Lok Access Device - intended as a sterile Recalled by...
The Issue: May shed contaminant particles into the urine specimen that may be...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: FLEXCERA SMILE -a Dental resins for the fabrication of artificial teeth...
The Issue: Manufactured in a non-FDA-registered manufacturing facility and product...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: FLEXCERA BASE -a Dental resins for the fabrication of artificial teeth...
The Issue: Manufactured in a non-FDA-registered manufacturing facility and product...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Semglee (insulin glargine) injection Recalled by Mylan Pharmaceuticals Inc...
The Issue: Labeling: Missing Label: label missing from some Semglee prefilled pens.
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Sufentanil Citrate Injection Recalled by Akorn, Inc. Due to Subpotent Drug:...
The Issue: Subpotent Drug: Out of specification for assay at the 30-month stability...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: ATTUNE REVISION POSTERIOR FEMORAL AUGMENT SZ 9 12MM-intended as a Recalled...
The Issue: May have adhesive residue on the posterior surface of the femoral augment,...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ATTUNE REVISION DISTAL FEMORAL AUGMENT SZ 6 4MM- Intended as Recalled by...
The Issue: May have adhesive residue on the posterior surface of the femoral augment,...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: BD Veritor Plus Analyzer - intended to provide rapid test Recalled by Becton...
The Issue: May have the potential to overheat and/or cause fire, the issue can occur...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: QC QUALITY CHOICE Recalled by Dr. Reddy's Laboratories, Inc. Due to Failed...
The Issue: Failed Dissolution Specifications
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: CVS Health Recalled by Dr. Reddy's Laboratories, Inc. Due to Failed...
The Issue: Failed Dissolution Specifications
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: equate Recalled by Dr. Reddy's Laboratories, Inc. Due to Failed Dissolution...
The Issue: Failed Dissolution Specifications
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Rugby Recalled by Dr. Reddy's Laboratories, Inc. Due to Failed Dissolution...
The Issue: Failed Dissolution Specifications
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Wal-Fex D Recalled by Dr. Reddy's Laboratories, Inc. Due to Failed...
The Issue: Failed Dissolution Specifications
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Dr. Reddys Recalled by Dr. Reddy's Laboratories, Inc. Due to Failed...
The Issue: Failed Dissolution Specifications
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Rite Aid Pharmacy Recalled by Dr. Reddy's Laboratories, Inc. Due to Failed...
The Issue: Failed Dissolution Specifications
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Leader Recalled by Dr. Reddy's Laboratories, Inc. Due to Failed Dissolution...
The Issue: Failed Dissolution Specifications
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Kroger Recalled by Dr. Reddy's Laboratories, Inc. Due to Failed Dissolution...
The Issue: Failed Dissolution Specifications
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: The Optima Coil System consists of an implantable embolization coil Recalled...
The Issue: Due to Label/Pouch mix-up. Pouches incorrectly labeled. Incorrect shelf...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: INTEGRA SURFIX ALPHA Screwdriver Torx 10 Recalled by Smith & Nephew, Inc....
The Issue: The affected screwdrivers are out of specification and may not mate with the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: eCareManager version 4.2.1 Recalled by Philips North America Llc Due to...
The Issue: eCareManager (eCM) Sentry Score software not approved for use
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.