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. 2,373 recalls have been distributed to South Dakota in the last 12 months.
Showing 22921–22940 of 27,558 recalls
Recalled Item: ADVIA Centaur¿¿ Systems HBc Total (HBcT) Kit. For In Vitro Recalled by...
The Issue: Increased imprecision and positive bias is observed with patient samples and...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Philips Expression Information Portal (IP5) Model 865471. The IP5 is...
The Issue: Frozen Display Numerics and Disabled Menu Keys after extended run time. This...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ADVIA Centaur¿ and ADVIA Centaur¿ XP and ADVIA Centaur¿ CP Recalled by...
The Issue: Stability of the ADVIA Centaur Cleaning Solution is not assured
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Prescription eyeglass safety lenses. Vision correction Recalled by Eyemart...
The Issue: Prescription eyeglass safety lenses did not meet specifications.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Omni Micro-electrode/ electrode for cobas b221 analyzer. The Roche...
The Issue: The default for normal values are inconsistent between cobas b 221 and other...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ARCHITECT Total T3 Reagent Kit (7K64) consists of: - 1 Recalled by Abbott...
The Issue: 17% of ARCHITECT Total T3 Reagent Kit, LN 7K64-20/-25 reagent lots 38901UI00...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ASSEMBLY Recalled by Intuitive Surgical, Inc. Due to Correction due to the...
The Issue: Correction due to the detection of a motor sensor failure in the Patient...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Persona The Personalized Knee System 2.5 mm Female Screw 48 Recalled by...
The Issue: The Persona 48mm X 2.5mm Female Screw is being recalled due to potential use...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Gardner-Wells wrenches are used in traction skull tongs for traction...
The Issue: The reason these devices are being withdrawn from the market by Instrumed is...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Traction tong replacement screws Recalled by Instrumed International, Inc....
The Issue: The reason these devices are being withdrawn from the market by Instrumed is...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Hudson RCI¿ Pediatric Anesthesia Breathing Circuits Recalled by Teleflex...
The Issue: The pediatric breathing circuits can crack prior to and during use.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: An external vein stripper is an extravascular device used to Recalled by...
The Issue: The reason these devices are being withdrawn from the market by Instrumed is...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Replacement screw non-springloaded traction tongs are skull tongs for...
The Issue: The reason these devices are being withdrawn from the market by Instrumed is...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: D'errico perforator drills are bone cutting and drilling instruments that...
The Issue: The reason these devices are being withdrawn from the market by Instrumed is...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: A zipser clamp is an instrument used to compress reduce Recalled by...
The Issue: The reason these devices are being withdrawn from the market by Instrumed is...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: McKenzie enlarging burrs are bone cutting and drilling instruments that...
The Issue: The reason these devices are being withdrawn from the market by Instrumed is...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Gardner-Wells traction tongs are skull tongs for traction used to Recalled...
The Issue: The reason these devices are being withdrawn from the market by Instrumed is...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Hudson cranial drill sets (w/ brace and 5 attachments) are Recalled by...
The Issue: The reason these devices are being withdrawn from the market by Instrumed is...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: A uterine tenaculum is a hook-like instrument used to seize Recalled by...
The Issue: The reason these devices are being withdrawn from the market by Instrumed is...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: VITROS 5600 Integrated System Recalled by Ortho-Clinical Diagnostics Due to...
The Issue: Ortho Clinical Diagnostics (OCD) identified an anomaly with Software Version...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.