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. 2,259 recalls have been distributed to South Dakota in the last 12 months.
Showing 46101–46120 of 47,632 recalls
Recalled Item: Instrumentation Laboratory ACL TOP (Base) PN 0000280000 ACL TOP is Recalled...
The Issue: Low Abnormal Fibrinogen Sample Reports as Normal and High Fibrinogen Sample...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Instrumentation Laboratory ACL TOP 700 CTS PN 0000280050 ACL TOP Recalled by...
The Issue: Low Abnormal Fibrinogen Sample Reports as Normal and High Fibrinogen Sample...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Instrumentation Laboratory ACL TOP CTS PN 0000280020 ACL TOP is a bench top...
The Issue: Low Abnormal Fibrinogen Sample Reports as Normal and High Fibrinogen Sample...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Instrumentation Laboratory ACL TOP 700 LAS PN 0000280030 ACL TOP Recalled by...
The Issue: Low Abnormal Fibrinogen Sample Reports as Normal and High Fibrinogen Sample...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: HALO Flex Energy Generators Manufactured by B¿RRX Medical (now Covidien)...
The Issue: Potential failure of HALO Energy Generator to enter "stand by" mode when...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Instrumentation Laboratory ACL TOP 500 CTS PN 0000280040 ACL TOP Recalled by...
The Issue: Low Abnormal Fibrinogen Sample Reports as Normal and High Fibrinogen Sample...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Newport HT70 and HT70 Plus Ventilators Recalled by Newport Medical...
The Issue: May emit a continuous high priority alarm and the ventilator may stop...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: The Brilliance 6 Recalled by Philips Medical Systems (Cleveland) Inc Due to...
The Issue: The patient support may move in an unintended manner if the foot switch...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Medstream 81" (206 cm) 20 Drop Standard bore Universal Administration...
The Issue: Devices leaking at the Y-site
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Crispy Punjabi Cookies Recalled by Deep Foods Inc Due to This recall has...
The Issue: This recall has been initiated due to Non-Declared Milk. This product may...
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: E-Z WIDER BARIATRIC CHAIR BED Recalled by Kreg Medical Inc. Due to An EZ...
The Issue: An EZ Wider bed (capacity of 1000 lb. safe working load collapsed during...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Sterile Empty Vial and Injector (30mL PCA vial) Recalled by Hospira, Inc....
The Issue: Reports of leaking during filling and administration.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: 100 ft roll of tubing inside a cardboard box. Medical Recalled by Steris...
The Issue: On 7/20/2012 the firm became aware that a lot of tubing was distributed by...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: PHADIA Varelisa Cardiolipin IgM Cardiolipin autoantibody immunological test...
The Issue: Customers were not following the labeled assay procedure. This was due to a...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Citalopram tablets USP Recalled by Dr. Reddy's Laboratories, Inc. Due to...
The Issue: Chemical Contamination: The product is being recalled due to complaints...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Citalopram tablets USP Recalled by Dr. Reddy's Laboratories, Inc. Due to...
The Issue: Chemical Contamination: The product is being recalled due to complaints...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Citalopram tablets USP Recalled by Dr. Reddy's Laboratories, Inc. Due to...
The Issue: Chemical Contamination: The product is being recalled due to complaints...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: GE Healthcare Optima XR 220amx 30kw Mobile X-ray System The Recalled by GE...
The Issue: GE Healthcare has become aware of a software issue on the interface of the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: GE Healthcare Optima XR 200 amx with Digital Upgrade. The Recalled by GE...
The Issue: GE Healthcare has become aware of a software issue on the interface of the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: GE Healthcare Optima XR 220amx 15kw Mobile X-Ray System The Recalled by GE...
The Issue: GE Healthcare has become aware of a software issue on the interface of the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.