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 23221–23240 of 27,558 recalls
Recalled Item: Name: Pasteur Pipets Recalled by ORIGIO, Inc Due to Identification of...
The Issue: Identification of packaging breach of the nylon pouch sterile barrier for...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Boston Scientific ENDOTAK RELIANCE¿ SG Recalled by Boston Scientific CRM...
The Issue: A review of manufacturing test records for Boston Scientific ENDOTAK...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: 5 mL Reaction Vessels (a consumable of the Abbott m2000sp Recalled by Abbott...
The Issue: Abbott Molecular identified that some of the 5 ml Reaction Vessels (RVs)...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Baxter MiniCap with Povidone-Iodine Solution Recalled by Baxter Healthcare...
The Issue: Inadequate iodine and packaging related defects.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Terumo¿ Advanced Perfusion System 1 100/120V AC Recalled by Terumo...
The Issue: An evaluation of the APS1 Operator Manual found that existing instructions...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: C-Series High Energy Linear Accelerator - Models: Novalis Tx Recalled by...
The Issue: Trend in reports of unexpected decrease in beam output in C-series High...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Terumo¿ Advanced Perfusion System 1 220/240V AC Recalled by Terumo...
The Issue: An evaluation of the APS1 Operator Manual found that existing instructions...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Non-Mydriatic Auto Fundus Camera. Model AFC-330. An ophthalmic camera for...
The Issue: Image taken by AFC-330 has a white spot which may affect diagnosis or...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Paragon Laboratory Management Recalled by McKesson Technologies, Inc. Due to...
The Issue: For Paragon Laboratory Management 12.1 and 12.1.1 releases, if used with...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: GE Healthcare Recalled by GE Healthcare, LLC Due to Partial loss of...
The Issue: Partial loss of monitoring with the CARESCAPE Monitor B850, B650 or B450....
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Ingenia 3.0T R5 Recalled by Philips Medical Systems, Inc. Due to For some...
The Issue: For some identified Ingenia systems shipped between December 2013 and March...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Ingenia 1.5T R5 Recalled by Philips Medical Systems, Inc. Due to For some...
The Issue: For some identified Ingenia systems shipped between December 2013 and March...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Ingenia 3.0T Recalled by Philips Medical Systems, Inc. Due to For some...
The Issue: For some identified Ingenia systems shipped between December 2013 and March...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Ingenia 1.5T Recalled by Philips Medical Systems, Inc. Due to For some...
The Issue: For some identified Ingenia systems shipped between December 2013 and March...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: EG-3630U Ultrasound Video Gastroscope EG-3830UT Ultrasound Video Gastroscope...
The Issue: Aspiration needles used in combination with Ultrasound Gastroscopes can...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: WaterLase iPlus Dental Laser System Recalled by Biolase Technology Inc Due...
The Issue: Biolase is recalling the WaterLase iPlus Dental Laser System because of a...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Zimmer EDI PERIARTICULAR PLATING SYSTEM CANCELLOUS BONE SCREW Recalled by...
The Issue: Two lots of screws were commingled. Screws with etching and machining for...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Pad-Pak and Pedi-Pak accessories for the HeartSine Samaritan PAD 300P...
The Issue: A small number of sealed foil pouches containing the electrodes were found...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: DATEX-OHMEDA S/5 SINGLE-WIDTH AIRWAY MODULE Recalled by GE Healthcare, LLC...
The Issue: Failure of the CO2 detector in Single-width Airway and Extension modules,...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Thermo Scientific VersaTREK REDOX 1 Recalled by Remel Inc Due to Bottles did...
The Issue: Bottles did not provide positive signals within the time frame of the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.