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. 2,554 recalls have been distributed to South Dakota in the last 12 months.
Showing 1221–1240 of 47,632 recalls
Recalled Item: LOGIQ P9 R4.5 ultrasound system with system software version R4.5.7....
The Issue: The Ultrasound-Guided Attenuation Parameter (UGAP) measurement data may...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Airvo 2 Recalled by Fisher & Paykel Healthcare, Ltd. Due to When...
The Issue: When unintentionally disconnected from power source, humidifier device (used...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: LOGIQ P10 series with software version R4.5.7 Model Number 5877534 Recalled...
The Issue: The Ultrasound-Guided Attenuation Parameter (UGAP) measurement data may...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: PERIFIX FX Continuous Epidural Anesthesia Tray with PERIFIX 17 Ga. Recalled...
The Issue: Potential for the lid of the catheter connector to be in the incorrect position.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Combined Spinal and Epidural Anesthesia Tray 2 Recalled by B BRAUN MEDICAL...
The Issue: Potential for the lid of the catheter connector to be in the incorrect position.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Combined Spinal and Epidural Anesthesia Tray Recalled by B BRAUN MEDICAL INC...
The Issue: Potential for the lid of the catheter connector to be in the incorrect position.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: PERIFIX FX Continuous Epidural Anesthesia Tray with PERIFIX 17 Ga. Recalled...
The Issue: Potential for the lid of the catheter connector to be in the incorrect position.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ESPOCAN Combined Spinal and Epidural Anesthesia Tray Recalled by B BRAUN...
The Issue: Potential for the lid of the catheter connector to be in the incorrect position.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: PERIFIX FX Continuous Epidural Anesthesia Tray with PERIFIX 17 Ga. Recalled...
The Issue: Potential for the lid of the catheter connector to be in the incorrect position.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: PERIFIX FX Continuous Epidural Anesthesia Tray Recalled by B BRAUN MEDICAL...
The Issue: Potential for the lid of the catheter connector to be in the incorrect position.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Design Options Recalled by B BRAUN MEDICAL INC Due to Potential for the lid...
The Issue: Potential for the lid of the catheter connector to be in the incorrect position.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: PERIFIX FX Continuous Epidural Anesthesia Tray Recalled by B BRAUN MEDICAL...
The Issue: Potential for the lid of the catheter connector to be in the incorrect position.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Design Options Recalled by B BRAUN MEDICAL INC Due to Potential for the lid...
The Issue: Potential for the lid of the catheter connector to be in the incorrect position.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: PERIFIX FX Continuous Epidural Anesthesia Tray Recalled by B BRAUN MEDICAL...
The Issue: Potential for the lid of the catheter connector to be in the incorrect position.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: PERIFIX FX Continuous Epidural Anesthesia Tray with PERIFIX 17 Ga. Recalled...
The Issue: Potential for the lid of the catheter connector to be in the incorrect position.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: PERIFIX FX Continuous Epidural Anesthesia Set Recalled by B BRAUN MEDICAL...
The Issue: Potential for the lid of the catheter connector to be in the incorrect position.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Lipton Green Tea Citrus. 16.9 ounce PET Bottle. sold as Recalled by Pepsico...
The Issue: Undeclared sugar in finished product-primary package does not the product...
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Azelaic Acid Gel Recalled by Glenmark Pharmaceuticals Inc., USA Due to CGMP...
The Issue: CGMP Deviations: Market complaints received for gritty texture (grainy)
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: InSure ONE Fecal Immunochemical Test. Labeled as follows: 1. Insure Recalled...
The Issue: InSure ONE failed sensitivity testing when used with Test Card Lot T241102,...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: MOSAIQ Oncology Information System Software Builds 3.1.3 Recalled by ELEKTA...
The Issue: When appending a care plan that contains one or more wave medication orders,...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.