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 2301–2320 of 47,632 recalls
Recalled Item: The HemoCue Glucose 201 Microcuvettes are designed for use with Recalled by...
The Issue: Glucose microcuvettes experienced transit time outside of limits, so...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Dexcom One+ Continuous Glucose Monitoring System Recalled by Dexcom, Inc....
The Issue: Defective foam or an assembly error may cause the receiver speaker to lose...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Dexcom One Continuous Glucose Monitoring System Recalled by Dexcom, Inc. Due...
The Issue: Defective foam or an assembly error may cause the receiver speaker to lose...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Dexcom G6 Glucose Receiver Recalled by Dexcom, Inc. Due to Defective foam or...
The Issue: Defective foam or an assembly error may cause the receiver speaker to lose...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Dexcom G7 Glucose Receiver Recalled by Dexcom, Inc. Due to Defective foam or...
The Issue: Defective foam or an assembly error may cause the receiver speaker to lose...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: BD TEXIUM CLOSED MALE LUER WITH FEMALE CAP Recalled by BD SWITZERLAND SARL...
The Issue: Sterile, single use closed system drug transfer devices, standalone or on...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: BD Texium Needle-Free Syringe: 3 mL Recalled by BD SWITZERLAND SARL Due to...
The Issue: Sterile, single use closed system drug transfer devices, standalone or on...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Baxter Novum IQ Syringe Pump Recalled by Baxter Healthcare Corporation Due...
The Issue: Baxter has identified a design issue which may cause the pump to detect the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: BD TEXIUM CLOSED MALE LUER WITH FEMALE CAP Recalled by BD SWITZERLAND SARL...
The Issue: Sterile, single use closed system drug transfer devices, standalone or on...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Alaris Pump Infusion Set: SmartSite Bag Access Non-Vented Bonded Texium...
The Issue: Sterile, single use closed system drug transfer devices, standalone or on...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: BD Texium: 3 mL Recalled by BD SWITZERLAND SARL Due to Sterile, single use...
The Issue: Sterile, single use closed system drug transfer devices, standalone or on...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Shore Lunch BREADING & BATTER MIX OVEN STYLE A savory Recalled by Homegrown...
The Issue: Undeclared Milk.
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Chlorthalidone Tablets Recalled by AvKARE Due to Failed Dissolution...
The Issue: Failed Dissolution Specifications
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Celecoxib Capsules Recalled by Alembic Pharmaceuticals Limited Due to...
The Issue: Presence of Foreign Tablets/Capsules; customer complaint found one Tadalafil...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Indomethacin Extended-Release Capsules USP Recalled by KVK Tech, Inc. Due to...
The Issue: cGMP deviations
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Phentermine Hydrochloride Capsules Recalled by KVK Tech, Inc. Due to cGMP...
The Issue: cGMP deviations
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: BiPAP A40 Ventilator. Used to provide noninvasive ventilation support for...
The Issue: This device does not indicate for use in patients with respiratory failure.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Brand Name: VITROS Recalled by Ortho-Clinical Diagnostics, Inc. Due to a...
The Issue: a software anomaly allows test results to be reported using Micro Tip and...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: BiPAP V30 Auto Ventilator. Intended to provide non-invasive ventilatory...
The Issue: This device does not indicate for use in patients with respiratory failure.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: BiPAP A30 Ventilators. Intended to provide noninvasive ventilation support...
The Issue: This device does not indicate for use in patients with respiratory failure.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.