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. 2,349 recalls have been distributed to South Dakota in the last 12 months.
Showing 27401–27420 of 27,558 recalls
Recalled Item: Pulset Arterial Blood Gas (ABG) sampling kit. Modified Kit Recalled by...
The Issue: Westmed is recalling Westmed ABG convenience kits containing TRIAD brand...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Pulset Arterial Blood Gas (ABG) sampling kit. Full Kit Recalled by Westmed...
The Issue: Westmed is recalling Westmed ABG convenience kits containing TRIAD brand...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Pulset Arterial Blood Gas (ABG) sampling kit. Full Kit Recalled by Westmed...
The Issue: Westmed is recalling Westmed ABG convenience kits containing TRIAD brand...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Pulset Arterial Blood Gas (ABG) sampling kit. Modified Kit Recalled by...
The Issue: Westmed is recalling Westmed ABG convenience kits containing TRIAD brand...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Pulset Arterial Blood Gas (ABG) sampling kit. Full Kit Recalled by Westmed...
The Issue: Westmed is recalling Westmed ABG convenience kits containing TRIAD brand...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Pulset Arterial Blood Gas (ABG) sampling kit. Full Kit Recalled by Westmed...
The Issue: Westmed is recalling Westmed ABG convenience kits containing TRIAD brand...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Pulset Arterial Blood Gas (ABG) sampling kit. Full Kit Recalled by Westmed...
The Issue: Westmed is recalling Westmed ABG convenience kits containing TRIAD brand...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: SteriGear Urinary Drain Bag with Fig Leaf Cover Recalled by SteriGear, LLC...
The Issue: SteriGear notifed customers of circumstances in which The Fig Leaf urinary...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Video Cytoscopes Recalled by Pentax of America Inc Due to This field action...
The Issue: This field action serves to retrospectively document the actions that were...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Video Bronchoscope Recalled by Pentax of America Inc Due to This field...
The Issue: This field action serves to retrospectively document the actions that were...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Video Naso pharyngo Laryngoscopes Recalled by Pentax of America Inc Due to...
The Issue: This field action serves to retrospectively document the actions that were...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: I-STAT EG7+ Cartridge Abbott Point of Care Recalled by Abbott Point Of Care...
The Issue: i-Stat EG7 cartridges may generate falsely depressed PCO2 results for...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ULTRA Fabric Reinforced Surgical Gown Recalled by Kimberly-Clark Corporation...
The Issue: The impacted product was not intended for commercial distribution to end users.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: M3150 Information Center Local Database Recalled by Philips Electronics...
The Issue: Potential for early component failure.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: TI Standard Polyaxial Screw Assembly 6.5MM x 55MM. Part # Recalled by...
The Issue: The recall was initiated because Alphatec Spine confirmed that the TI...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: BCS(R) Behring Coagulation System Recalled by Siemens Healthcare...
The Issue: Firm has confirmed that if the Cleaner SCS vial becomes empty after...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Canon Solid State X-ray Imager (Flat Panel/Digital Imager) Recalled by Canon...
The Issue: Screws holding the 55REF circuit board are loosening and roaming inside of...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Medtronic 0-arm Imaging System with Software Version 3.1.1 Recalled by...
The Issue: Software Version 3.1.1 does not meet navigational accuracy.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: 00780304001 MIS 12/14 Slotted Femoral Head Provisional -3.5X36 00780304002...
The Issue: Surgical technique instructions for the Versys and Slotted Provisional...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: 00780303201 MIS 12/14 Slotted Femoral Head Provisional -3.5X32 00780303202...
The Issue: Surgical technique instructions for the Versys and Slotted Provisional...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.