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. 2,396 recalls have been distributed to South Dakota in the last 12 months.
Showing 19081–19100 of 47,632 recalls
Recalled Item: VitreQ 20G VFI Cannula-.D03 GTIN: 8719214221485 Recalled by Vitreq Bv Due to...
The Issue: Microscopic tears of the sterile pouch may compromise sterility
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: VitreQ 23G Blunt Needles with luer-lock connector-.D05 GTIN: 8719214221621...
The Issue: Microscopic tears of the sterile pouch may compromise sterility
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: VitreQ 25G Silicone Tipped Cannula-.D01 GTIN: 8719214221522 Recalled by...
The Issue: Microscopic tears of the sterile pouch may compromise sterility
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: VitreQ 25G VFI Cannula-.D03 GTIN: 8719214221447 Recalled by Vitreq Bv Due to...
The Issue: Microscopic tears of the sterile pouch may compromise sterility
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: VitreQ 25G Pick Needles-.D04 GTIN: 8719214221607 Recalled by Vitreq Bv Due...
The Issue: Microscopic tears of the sterile pouch may compromise sterility
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: VitreQ 25G PFC Injection Needle-.D01 GTIN: 8719214221386 Recalled by Vitreq...
The Issue: Microscopic tears of the sterile pouch may compromise sterility
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: (1)VitreQ 25G BF Blunt Needles-BF25.D51 GITN: 8719214221164 (2) VitreQ 25G...
The Issue: Microscopic tears of the sterile pouch may compromise sterility
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Ketorolac Tromethamine Injection Recalled by Hikma Pharmaceuticals USA Inc....
The Issue: Presence of Particulate Matter: particles identified as polydimethylsiloxane...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Ketorolac Tromethamine Injection Recalled by Hikma Pharmaceuticals USA Inc....
The Issue: Presence of Particulate Matter: particles identified as polydimethylsiloxane...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: AMS 700 100 mL Recalled by Boston Scientific Corporation Due to A labeling...
The Issue: A labeling discrepancy incorrectly labeled AMS 700 100mL Conceal Low Profile...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Recalled by Quest Medical, Inc. Due to Additive and Arrest Agent Labels on...
The Issue: Additive and Arrest Agent Labels on the MPS Top Cover Replacement Kit, a...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: 2.4MM TI VA LOCKING SCREW STARDRIVE 18MM STERILE Recalled by Synthes, Inc....
The Issue: There is a possibility that the inner cap could open when the outer cap is...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: 2.4MM TI VA LOCKING SCREW STARDRIVE 24MM STERILE Recalled by Synthes, Inc....
The Issue: There is a possibility that the inner cap could open when the outer cap is...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Microbiologics QC Sets and Panels Recalled by Microbiologics Inc Due to The...
The Issue: The recommended hydration fluid for the 8180 Gram-Positive Blood Culture...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: 2.4MM TI VA LOCKING SCREW STARDRIVE 10MM STERILE Recalled by Synthes, Inc....
The Issue: There is a possibility that the inner cap could open when the outer cap is...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: VITROS Chemistry Products Calibrator Kit 2- IVD calibrator for VITROS...
The Issue: Potential for Negatively Biased Na+ Urine Results Using Several Lots of...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: 2.4MM TI VA LOCKING SCREW STARDRIVE 16MM STERILE Recalled by Synthes, Inc....
The Issue: There is a possibility that the inner cap could open when the outer cap is...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Centricity Universal Viewer 6.0 Recalled by GE Healthcare, LLC Due to...
The Issue: Centricity Universal Viewer measurements saved into a DICOM Grayscale...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: 2.4MM TI VA LOCKING SCREW STARDRIVE 12MM STERILE Recalled by Synthes, Inc....
The Issue: There is a possibility that the inner cap could open when the outer cap is...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: NORepinephrine Bitartrate 8 mg added to 250 mL 5% Dextrose Recalled by...
The Issue: Subpotent Drug
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.