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. 2,365 recalls have been distributed to South Dakota in the last 12 months.
Showing 24001–24020 of 27,558 recalls
Recalled Item: AOA Distalizer Lock Nut Screw Recalled by Allesee Orthodontic Appliances Due...
The Issue: The Lock Nut component of the Jet appliances may be missing the screw...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: L S-ROM Noiles Rotating Hinge Recalled by DePuy Orthopaedics, Inc. Due to...
The Issue: DePuy Orthopaedics has identified the potential for holes to develop in the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: RS-ROM Noiles Rotating Hinge Recalled by DePuy Orthopaedics, Inc. Due to...
The Issue: DePuy Orthopaedics has identified the potential for holes to develop in the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: L S-ROM Noiles Rotating Hinge Recalled by DePuy Orthopaedics, Inc. Due to...
The Issue: DePuy Orthopaedics has identified the potential for holes to develop in the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: MEDITECH Microbiology Recalled by Medical Information Technology, Inc. Due...
The Issue: Potential for erroneous result reporting.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: DeRoyal(R) LIMB HOLDERS Recalled by DeRoyal Industries Inc Due to Moldy...
The Issue: Moldy smell in product
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: PENTARAY NAV High-Density Mapping Catheter and PENTARAY NAV ECO Catheter...
The Issue: Biosense Webster is recalling the PentaRay Nav Catheter because it has the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: VITROS TT4 Calibrator For the quantitative measurement of total thyroxine...
The Issue: Total T4 Calibrators and Reagent Packs may have calibration failures or low...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Heparin I.V. Flush Syringe is available is pre-filled polypropylene syringes...
The Issue: The bar code that is printed on the Master Carton label does not correspond...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: FreeStyle Blood Glucose Monitors System. For in vitro diagnostic use...
The Issue: Abbott Diabetes Care has identified through internal testing and...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: FreeStyle Flash Blood Glucose Monitors System. Meter made in China Recalled...
The Issue: Abbott Diabetes Care has identified through internal testing and...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Oxoid Vancomycin 30 mcg Recalled by Remel Inc Due to Some of the discs may...
The Issue: Some of the discs may not be impregnated with the antibiotic.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Philips HeartStart MRx Monitor/Defibrillator Model numbers: M3535A Recalled...
The Issue: MRx may display a Red X in the Ready For Use (RFU) indicator during...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ADVIA Centaur XP Immunoassay system Recalled by Siemens Healthcare...
The Issue: Instrument Cover Gas Spring failures. Over time, the gas spring may lose its...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: HeartStart MRx Defibrillator/Monitor M3538A Lithium Ion Batteries Revision J...
The Issue: Philips HeartStart MRx Monitor/Defibrillator, when operating on battery...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: GemStar Docking Station Recalled by Hospira Inc. Due to There are two...
The Issue: There are two situations that may occur when using the GemStar Docking...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: HeartStart MRx Monitor/Defibrillator Recalled by Philips Medical Systems,...
The Issue: A component of the MRx Processor Board may be susceptible to damage from...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Philips HeartStart MRx Monitor/Defibrillator Models: M3535A and M3536A with...
The Issue: When the HeartStart MRx.is used with the Q-CPR Meter in defibrillation mode,...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Philips HeartStart MRx Monitor/Defibrillator Recalled by Philips Medical...
The Issue: ECG trunk cable and connector block of the MRx could be susceptible to...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Philips HeartStart XL Recalled by Philips Medical Systems, Inc. Due to...
The Issue: Philips HeartStart XL may experience a power board failure causing failure...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.