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. 2,491 recalls have been distributed to South Dakota in the last 12 months.
Showing 10981–11000 of 27,558 recalls
Recalled Item: 30" (76 cm) Appx 3.2 ml Recalled by ICU Medical, Inc. Due to Potential for...
The Issue: Potential for spinning versions of male luers to exhibit leaks due to a...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Spinning Spiros Closed Male Luer Recalled by ICU Medical, Inc. Due to...
The Issue: Potential for spinning versions of male luers to exhibit leaks due to a...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: 31" (78 cm) Appx 3.4 ml Recalled by ICU Medical, Inc. Due to Potential for...
The Issue: Potential for spinning versions of male luers to exhibit leaks due to a...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: 3mL Syringe w/Spinning Spiros Recalled by ICU Medical, Inc. Due to Potential...
The Issue: Potential for spinning versions of male luers to exhibit leaks due to a...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Spinning Spiros Recalled by ICU Medical, Inc. Due to Potential for spinning...
The Issue: Potential for spinning versions of male luers to exhibit leaks due to a...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: AltiVate Reverse Small Socket Insert Recalled by Encore Medical, LP Due to...
The Issue: Product mislabeled. Use may result in a delay in surgery, stopping of...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Langston Dual Lumen Catheter. Recalled by Vascular Solutions, Inc. Due to...
The Issue: The inner lumen of the Langston catheter may separate from the hub during...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Langston Dual Lumen Catheter Recalled by Vascular Solutions, Inc. Due to The...
The Issue: The inner lumen of the Langston catheter may separate from the hub during...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Olympus CHF-CB30S Choledoscope Intended Use: The device was designed to...
The Issue: The CHF-CB30S Device did not have a 510(k) clearance. Additionally, the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Langston Dual Lumen Catheter. Recalled by Vascular Solutions, Inc. Due to...
The Issue: The inner lumen of the Langston catheter may separate from the hub during...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Langston Dual Lumen Catheter. Recalled by Vascular Solutions, Inc. Due to...
The Issue: The inner lumen of the Langston catheter may separate from the hub during...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: DISCOVERY ULTRA Advanced Staining System (RUO-Research Use Only) Material...
The Issue: Potential for Fluid leaks within the instruments, creating an electrical...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Pediatric Nephrostomy Stent Set Recalled by Cook Inc. Due to The indwell...
The Issue: The indwell time for the Percutaneous Neonatal Pigtail Nephrostomy Set and...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Percutaneous Neonatal Pigtail Nephrostomy Set Recalled by Cook Inc. Due to...
The Issue: The indwell time for the Percutaneous Neonatal Pigtail Nephrostomy Set and...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Ultrasound Navigation Software 1.0 and Ultrasound Integration Software for...
The Issue: Brainlab Ultrasound Navigation Software does not support the modification of...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: BenchMark ULTRA Advanced Staining System (IVD)- Material Number: 05342716001...
The Issue: Potential for Fluid leaks within the instruments, creating an electrical...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: PermaFlo Flowable Composite 948 Shade: A2 - Product Usage: Recalled by...
The Issue: Due to a potential manufacturing issue (cross contamination), composite is...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Olympus Medical Systems Corporation (OMSC) Evis Exera II Bronchovideoscope...
The Issue: The BF-Q180 bronchoscope is being recalled because it does not have a 510(k)...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: 30" (76 cm) Appx 5.5 mL 20 Drop Admin Set w/Integrated Clave Drip Chamber...
The Issue: Potential for spinning versions of male luers to exhibit leaks due to a...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: VACUETTE TUBE 5 mL CAT Serum Separator Clot Activator Recalled by Greiner...
The Issue: Blood collection tubes experienced an issue with separation and clotting
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.