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. 2,365 recalls have been distributed to South Dakota in the last 12 months.
Showing 23781–23800 of 27,558 recalls
Recalled Item: e.cam camera system. Emission Computed Tomography System used to detect...
The Issue: Siemens Medical Solutions USA, Inc. has received reports indicating the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Gluma Desensitizer Power Gel Product Usage: Usage: This is a Recalled by...
The Issue: The firm discovered that the Gluma Desensitizer Power Gel can be...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Monoswift¿ PGCL [poly (glycolide-co-caprolactone)] Absorbable Surgical...
The Issue: CP Medical, Inc., is recalling one lot of Monoswift PGCL [poly...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Alaris Pump model 8100 with software version 9.1.18 and software Recalled by...
The Issue: CareFusion is recalling the Alaris Pump model 8100 version 9.1.18 because it...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ExploR 7x26mm Modular Radial Stem Recalled by Biomet, Inc. Due to This lot...
The Issue: This lot of the ExploR Modular Radial Stem may be missing the wedge ramp...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Synthes Matrix Mandible Short Cut Plate Cutter Synthes Matrix Mandible...
The Issue: It was discovered internally that the face of the Synthes Matrix Mandible...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: HAMILTON-G5 Ventilator with software versions between V2.00 and V2.31....
The Issue: Ventilation and alarms of a HAMILTON-G5 ventilator can be suppressed...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Bausch & Lomb Recalled by Bausch & Lomb Inc- Greenville Solutions Plant Due...
The Issue: Out of specification results for one of the two disinfectants.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: RetractaBed Recalled by Med-Mizer, Inc. Due to All configurations of the SS...
The Issue: All configurations of the SS Retractabed, Clinical Contour, made prior to...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: RetractaBed Recalled by Med-Mizer, Inc. Due to All configurations of the SS...
The Issue: All configurations of the SS Retractabed, Clinical Contour, made prior to...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: RetractaBed Recalled by Med-Mizer, Inc. Due to All configurations of the SS...
The Issue: All configurations of the SS Retractabed, Clinical Contour, made prior to...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: McKesson Radiology-PACS. McKesson Radiology is a medical image and...
The Issue: High priority alert icon was not displayed in the Study List when there are...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: APTIMA Urine Collection Kit Recalled by Gen-Probe Inc Due to Incorrect...
The Issue: Incorrect labeling was used on each pouch of the affected lots of APTIMA...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Alere INRatio2 PT/INR Professional Test Strips Recalled by Alere San Diego,...
The Issue: Test Strips may report an inaccurately low INR result. Several patients had...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Tissue-Tek PARAFORM PROC/EMB/MEDIUM Recalled by Sakura Finetek USA Inc Due...
The Issue: This Lot has variations in melting temperature.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: DePuy Synthes Craniomaxillofacial Distraction System (AB Distractor Bodies...
The Issue: DePuy Synthes is initiating a recall of certain lots of the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: HeartWare HVAD Pump Implant Kit (Heartware Ventricular Assist Device) -...
The Issue: Patients and caregivers are instructed that if a battery does not provide...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Maquet PowerLED 700. Product Usage Recalled by Maquet Medical Systems USA...
The Issue: Maquet has identified an issue with the Maquet PowerLED 700 (certain serial...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: EZPass Suture Retriever Recalled by Biomet, Inc. Due to The nitinol wire or...
The Issue: The nitinol wire or monofilament may buckle within the EZPass Suture Passer...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: EZPass Passer Recalled by Biomet, Inc. Due to The nitinol wire or...
The Issue: The nitinol wire or monofilament may buckle within the EZPass Suture Passer...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.