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. 2,260 recalls have been distributed to South Dakota in the last 12 months.
Showing 44601–44620 of 47,632 recalls
Recalled Item: McKesson Anesthesia Care Product Usage: The McKesson Anesthesia Care system...
The Issue: There was an occurrence where the patient case data did not match the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: The GemStar Pump is a small and lightweight Recalled by Hospira Inc. Due to...
The Issue: The proximal and distal pressure sensor calibration can drift resulting in...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: The GemStar Pump is a small and lightweight Recalled by Hospira Inc. Due to...
The Issue: The proximal and distal pressure sensor calibration can drift resulting in...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Vitrea¿ CT Brain Perfusion made available in various configurations under...
The Issue: Vital Images, Inc. (Vital Images) received one report about potential user...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: IS3000 USER MANUAL for Intuitive Surgical da Vinci Si Surgical Recalled by...
The Issue: Revised instructions for users of the da Vinci S, Si and Si-e systems with...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: IS2000 USER MANUAL for Intuitive Surgical da Vinci S Surgical System...
The Issue: Revised instructions for users of the da Vinci S, Si and Si-e systems with...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ACIST Medical Systems Inc. The ACIST Angiographic Injection System is...
The Issue: ACIST Medical Systems is issuing a voluntary recall notice for three...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: IMPAX CV Reporting Cardiac Catheterization module and IMPAX CV Outbound...
The Issue: Baseline pulmonary capillary wedge (PCW) pressure values from IMPAX CV...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Magnesium Sulfate 2 grams in Dextrose 5% for Injection Recalled by Med Prep...
The Issue: Non-Sterility; mold contamination
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: All Compounded Products Recalled by Med Prep Consulting, Inc. Due to Lack of...
The Issue: Lack of Assurance of Sterility; potential for mold contamination
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Seasonale(R) (Levonorgestrel/Ethinyl Estradiol Tablets) Recalled by Teva...
The Issue: Failed Impurity/Degradation Specification; an impurity identified as...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Camrese(TM) (Levonorgestrel/Ethinyl Estradiol Tablets) Recalled by Teva...
The Issue: Failed Impurity/Degradation Specifications; an impurity identified as...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: VITROS Chemistry Products PHBR (Phenobarbital) Slides Recalled by...
The Issue: Ortho Clinical Diagnostics (OCD) received customer complaints of...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: The Oxford Partial Knee Recalled by Synvasive Technology Inc Due to Biomet...
The Issue: Biomet part # 506076, lot 928182 was received from Synvasive Technology...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Edwards Lifesciences Duraflo coated Femoral Cannula. Product Usage: The...
The Issue: Two unsealed pouches were found at an Edwards' distribution location in...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Precise Treatment Table. To be used as part of radiation Recalled by Elekta,...
The Issue: The Column rotation can accidentally be moved to a different position which...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Sunchang Ssamjang Sesame and Garlic Seasoned Bean Paste 500 g Recalled by...
The Issue: Sesame and Garlic Flavored Mixed Soy Bean Paste contains peanut powder which...
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: NewChapter Probiotic Elderberry Recalled by New Chapter, Inc. Due to...
The Issue: The product may contain an undeclared allergen soy
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: epoc BGEM Test Card (Catalogue number CT-1004-00-00). quantitative testing...
The Issue: This recall is being initiated because the affected lots of this product may...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: SLIDERPREP PLUS SLIDE PREPARATION CENTRIFUGE. Produce a monolayer of cells...
The Issue: Separation Technology, Inc. recalled SlidePrep Plus Cytology Centrifuges...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.