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. 2,512 recalls have been distributed to South Dakota in the last 12 months.
Showing 9541–9560 of 47,632 recalls
Recalled Item: Express Mini 500 Dry Seal Chest Drain Recalled by Atrium Medical Corporation...
The Issue: The Instructions for Use (IFU) for the Pneumostat Chest Drain Valve and the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Color Cuff Single Port Recalled by Stryker Sustainability Solutions Due to...
The Issue: Increased incidence of disposable tourniquet cuffs "not able to achieve...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Atrium Pneumostat Chest Drain Valve Recalled by Atrium Medical Corporation...
The Issue: The Instructions for Use (IFU) for the Pneumostat Chest Drain Valve and the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Heparin Sodium Injection Recalled by Sagent Pharmaceuticals Inc Due to...
The Issue: Labeling: Not elsewhere classified
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: BODYARMOR SportWater 24/700mL Recalled by BA Sports Nutrition, LLC Due to...
The Issue: Potential for plastic pieces in product
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Omega Medical Imaging Elevating Monitor Suspension Recalled by Omega Medical...
The Issue: An actuator separated from the pivot mechanism on a lower monitor boom...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: BioPlex 2200 Recalled by Bio-Rad Laboratories, Inc. Due to APLS IgM reagent...
The Issue: APLS IgM reagent kits were packaged with the incorrect conjugate, which...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Bard Mission Disposable Core Biopsy Instrument Kit: 16G x 10CM Recalled by...
The Issue: The external diameter of the biopsy instrument is larger than the internal...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Monaco RTP System. Used to make treatment plans for patients Recalled by...
The Issue: Re-optimization, after adding contours without forced density outside the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: FujiFilm FDR AQRO (Model DR-XD1000)- A digital mobile X-ray system Recalled...
The Issue: Arm which holds the tube head in place is susceptible to breaking, if the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Delsam Pharma's Artificial Eye Ointment (Mineral Oil 15% Recalled by Global...
The Issue: Non-Sterility: FDA analysis found unopened tubes to be contaminated with...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Unguentine Original Maximum Strength Pain Relieving/Antiseptic Ointment...
The Issue: CGMP DEVIATIONS
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Alcolado Relampago (menthol 1% Recalled by Ecometics, Inc. Due to CGMP...
The Issue: CGMP DEVIATIONS
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Activator Concentrate (sodium fluoride 0.96% in Activator) 1 fl. Oz Recalled...
The Issue: CGMP DEVIATIONS
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Vencedor medicated balm (capsaicin 0.028%) 1.5 oz. (43g) tubes Recalled by...
The Issue: CGMP DEVIATIONS
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Unguentine Original Ointment for Burns (Camphor 3.0% Recalled by Ecometics,...
The Issue: CGMP DEVIATIONS
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Soltice Quick-RUB (Menthol 5.1% Recalled by Ecometics, Inc. Due to CGMP...
The Issue: CGMP DEVIATIONS
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Nose Better Gel (0.75% Camphor Recalled by Ecometics, Inc. Due to CGMP...
The Issue: CGMP DEVIATIONS
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Fentanyl 1 Recalled by SCA Pharmaceuticals Due to Subpotent Drug
The Issue: Subpotent Drug
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Tobii Dynavox TD I-110 Speech Device-tablet style speech generating device...
The Issue: Problem maintaining the stable placement of the battery may come loose from...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.