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. 2,521 recalls have been distributed to South Dakota in the last 12 months.
Showing 6561–6580 of 27,558 recalls
Recalled Item: DuraLife Autoclavable Double Swivel Elbow Recalled by Smiths Medical ASD...
The Issue: DuraLife devices instructions for cleaning and sterilization have been...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Beckman Coulter Bicarbonate Recalled by Beckman Coulter Inc. Due to There is...
The Issue: There is a potential for a decrease in calibration ODs for Bicarbonate...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Beckman Coulter Bicarbonate Recalled by Beckman Coulter Inc. Due to There is...
The Issue: There is a potential for a decrease in calibration ODs for Bicarbonate...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: DuraLife Autoclavable Silicone Extension Tube Recalled by Smiths Medical ASD...
The Issue: DuraLife devices instructions for cleaning and sterilization have been...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: DuraLife Autoclavable Silicone Extension Tube Recalled by Smiths Medical ASD...
The Issue: DuraLife devices instructions for cleaning and sterilization have been...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Beckman Coulter Bicarbonate Recalled by Beckman Coulter Inc. Due to There is...
The Issue: There is a potential for a decrease in calibration ODs for Bicarbonate...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: BD Pyxis MedStation ES (Med ES Main) Recalled by CareFusion 303, Inc. Due to...
The Issue: Automated dispensing cabinet software is experiencing: 1) ES device download...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Draeger Infinity M300 and M300+ Recalled by Draeger Medical Systems, Inc....
The Issue: The software on the Infinity CentralStation drops peaks on narrow waveforms...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Draeger Infinity CentralStation (ICS) Recalled by Draeger Medical Systems,...
The Issue: The software on the Infinity CentralStation drops peaks on narrow waveforms...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: GEO Instrument Kit for EPS Plate Recalled by GRAMERCY EXTREMITY ORTHOPEDICS...
The Issue: Instrument Kits for EPS plates may contain drill guides with incorrect drill...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Pilot COVID-19 At-Home Test Recalled by SD Biosensor, Inc. Due to The liquid...
The Issue: The liquid buffer component in the affected test kit lots was determined to...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: greiner bio-one VACUETTE TUBE 6 ml K3E K3EDTA Recalled by Greiner Bio-One...
The Issue: Some of the tubes may be incorrectly labeled.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Hill-Rom pro+ mattress Recalled by Baxter Healthcare Corporation Due to...
The Issue: There is a potential for mattress cover damage (delamination) which may...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Eye and Ear Dropper Recalled by Apothecary Products, LLC Due to Potential...
The Issue: Potential for glass dropper to have glass particulate on the outside surface...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Medicine Dropper Recalled by Apothecary Products, LLC Due to Potential for...
The Issue: Potential for glass dropper to have glass particulate on the outside surface...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: DYND3000xxP Series - Flexible Laryngeal Mask Airway Packs Recalled by...
The Issue: The case and each (i.e. packet) labels for the DYND3000xxP series do not...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Immundiagnostik IDK Lactoferrin ELISA- In vitro enzyme immunoassay intended...
The Issue: Marketed without a 510k
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: TDHisto/Cyto - A software product used for managing medical information...
The Issue: In a specific use case, when printing labels for slides, some labels may...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: GEM NEUROTUBE Recalled by Baxter Healthcare Corporation Due to The product...
The Issue: The product is brittle and potentially crumbling upon handling or when being...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: JOURNEY II UNI XLPE TIBIA INSERT MEDIAL SZ 7-8 8MM Recalled by Smith &...
The Issue: A mispack occurred during the manufacturing process, resulting in the box...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.