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. 2,311 recalls have been distributed to South Dakota in the last 12 months.
Showing 36441–36460 of 47,632 recalls
Recalled Item: GLUTATHIONE 200MG/ML (STERILE WATER) (30ML Recalled by Advanced Physician...
The Issue: Lack of Assurance of Sterility
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: ESTRADIOL VALERATE (10ML VIAL) SESAME OIL 45MG/ML INJECTABLE Recalled by...
The Issue: Lack of Assurance of Sterility
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: NANDROLONE DECANOATE (SESAME OIL) 100ML VIAL 200MG/ML INJECTABLE Recalled by...
The Issue: Lack of Assurance of Sterility
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: DMSO (STERILE WATER) SOLUTION -50ML VIAL 50% INJECTABLE Recalled by Advanced...
The Issue: Lack of Assurance of Sterility
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: NANPYRIDOXINE (STERILE WATER) 30ML 50MG/ML INJECTABLE Recalled by Advanced...
The Issue: Lack of Assurance of Sterility
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: PROcise XP Wand with Integrated Cable Product Usage: Recalled by ArthroCare...
The Issue: Potential component failure resulting in inoperability
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: EVAC 70 XTRA with Integrated Cable Product Usage: Recalled by ArthroCare...
The Issue: Potential component failure causing device inoperability
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: MedTest DX Control Reconstitution Fluid Kit configuration: 20 x 5 Recalled...
The Issue: Vial to vial variation in the fill volume that could affect control recovery...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Cell Search Circulating Tumor Kit. Intended for the enumeration of Recalled...
The Issue: Complaints of the presence of artifacts that appears as small bead like...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Syngo.via and Syngo.x Recalled by Siemens Medical Solutions USA, Inc Due to...
The Issue: measurements drawn on the 2nd and subsequent images of the series are not...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Philips Ultrasound Recalled by Philips Ultrasound, Inc. Due to Philips...
The Issue: Philips Healthcare has discovered a problem in the Philips Ultrasound...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: The Optigun Ratchet is a hand-held cement gun for use Recalled by BIOMET...
The Issue: The pin which maintains the knob button, may disconnect and become lost....
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: LapSac Surgical Tissue Pouch. The current intended use for the Recalled by...
The Issue: Includes Information not stated in the intended use.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Lifesaver Single Patient Use Manual Resuscitator Product Usage: The Hudson...
The Issue: The intake port may be blocked which can cause the bag to fail to fill.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: 3.7mm Cannulated Locking Screws and 3.7mm Cannulated Conical Screws Recalled...
The Issue: Certain lots of the 3.7mm Cannulated Locking Screws and 3.7mm Cannulated...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Alaris PC unit model 8015 Recalled by CareFusion 303, Inc. Due to An issue...
The Issue: An issue with the cancel functionality used during atypical infusion...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: 3.2 mm Cannulated Drill Bit/ QC 170 mm 2.7 Cannulated Recalled by Synthes,...
The Issue: affected parts and lots of the Cannulated Drill Bits have the potential to...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: SEDASYS Computer-Assisted Personalized Sedation System Recalled by Ethicon...
The Issue: Ethicon has found that disinfecting methods not specified in the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Fentanyl Citrate Inj. Recalled by West-Ward Pharmaceutical Corp. Due to...
The Issue: Failed Impurities/Degradation Specifications; 12 month stability testing...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Optilite Analyser Recalled by The Binding Site Group, Ltd. Due to Potential...
The Issue: Potential risk of the Optilite lid/cover falling suddenly and causing injury...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.