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. 2,554 recalls have been distributed to South Dakota in the last 12 months.
Showing 2121–2140 of 47,632 recalls
Recalled Item: Brand Name: NIO-A Product Name: NIO Intraosseous Device Adult Model/Catalog...
The Issue: Due to manufacturing error, Intraosseous device built-in stabilizer may not...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Bornstein Frozen Shrimp Meat Recalled by Bornstein Seafoods Inc Due to...
The Issue: The recall was the result of the firm's routine sampling program and...
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Zvu Anorectal Manometry Procedure Kit Recalled by Diversatek Healthcare Due...
The Issue: Anorectal manometry procedure kit outer kit label is mislabeled with an...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Brand Name: T4 Total ELISA Product Name: T4 Total ELISA Recalled by DRG...
The Issue: An incoming complaint reported that the expiration date on the kit box label...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Azurion 7 M20. Fluoroscopic X-Ray System. Recalled by PHILIPS MEDICAL...
The Issue: Potential for bolts connecting the gearbox to the mounting flange of the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ADVIA¿ 120/2120/2120i 3-in-1 TESTpoint Control (ABN2 Control) Recalled by...
The Issue: Products have the incorrect platelet (PLT) value assignments for the ADVIA...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ADVIA¿ 120/2120/2120i 3-in-1 TESTpoint Control (Norm Control) Recalled by...
The Issue: Products have the incorrect platelet (PLT) value assignments for the ADVIA...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ADVIA¿ 120/2120/2120i 3-in-1 TESTpoint Control (ABN1 Control) Recalled by...
The Issue: Products have the incorrect platelet (PLT) value assignments for the ADVIA...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ADVIA¿ 120/2120/2120i SETpoint Calibrator Recalled by Siemens Healthcare...
The Issue: Products have the incorrect platelet (PLT) value assignments for the ADVIA...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: UROSKOP Omnia. Model Number: 10094910 Recalled by Siemens Medical Solutions...
The Issue: A resistor in the frequency inverter may strongly overheat potentially...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: UROSKOP Omnia Max. Model Number: 10762473 Recalled by Siemens Medical...
The Issue: A resistor in the frequency inverter may strongly overheat potentially...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Peak Cocktails Blood Orange Spritz 8.4 fl oz aluminum cans Recalled by Peak...
The Issue: Overpressurization leading to exploding cans
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Hamilton C6 (ESM Board PN 10144626 UDI-DI code: Recalled by Hamilton Medical...
The Issue: A mechanical defect on a printed circuit board (PCB) as a result of PCB...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: SwabCap Disinfecting Cap for Needlefree Connectors: SwabSleeve Recalled by...
The Issue: Due to a manufacturing issue, disinfecting cap for needle-free connectors...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Bravo CF capsule delivery device Recalled by Given Imaging Ltd. Due to It...
The Issue: It has been determined that misapplied adhesive on the Bravo CF capsule...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Recalled by C.R. Bard Inc Due to Cather packaging may contain the incorrect...
The Issue: Cather packaging may contain the incorrect French size.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: BD Heyman Follower Straight Tip for following sizes: 10Fr - Recalled by C.R....
The Issue: Cather packaging may contain the incorrect French size.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: BD Heyman Follower Coude Tip for following sizes: 12Fr - Recalled by C.R....
The Issue: Cather packaging may contain the incorrect French size.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: KETAmine Hydrochloride Injection Recalled by Tailstorm Health INC Due to...
The Issue: Lack of Assurance of Sterility: A recent FDA inspection revealed concerns...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: LIDOcaine HCL Sterile Injection Recalled by Tailstorm Health INC Due to Lack...
The Issue: Lack of Assurance of Sterility: A recent FDA inspection revealed concerns...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.