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. 2,429 recalls have been distributed to South Dakota in the last 12 months.
Showing 18301–18320 of 47,632 recalls
Recalled Item: Levetiracetam Tablets USP 750 mg 120-count bottles Recalled by Aurobindo...
The Issue: CGMP Deviations: Products were manufactured in a processing area in which...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Oxycodone and Acetaminophen Tablets Recalled by Aurobindo Pharma USA Inc....
The Issue: CGMP Deviations: Products were manufactured in a processing area in which...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Mirtazapine Tablets Recalled by Aurobindo Pharma USA Inc. Due to CGMP...
The Issue: CGMP Deviations: Products were manufactured in a processing area in which...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Simvastatin Tablets Recalled by Aurobindo Pharma USA Inc. Due to CGMP...
The Issue: CGMP Deviations: Products were manufactured in a processing area in which...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Acetaminophen and Codeine Phosphate Tablets Recalled by Aurobindo Pharma USA...
The Issue: CGMP Deviations: Products were manufactured in a processing area in which...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: X12+ and patient cable for the X12+ Telemeter with the Recalled by WELCH...
The Issue: Impacted Welch Allyn products may not meet the Defibrillation Withstand...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Lead diagnostic electrocardiograph under the following device names: ELI 10...
The Issue: Impacted Welch Allyn products may not meet the Defibrillation Withstand...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Surveyor S12/S19 and patient cable for the S12/S19 Bedside Monitor Recalled...
The Issue: Impacted Welch Allyn products may not meet the Defibrillation Withstand...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Replaceable lead set for the Wireless Acquisition Module (WAM) Recalled by...
The Issue: Impacted Welch Allyn products may not meet the Defibrillation Withstand...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: T12. Incorporates wireless electrocardiographic technology to achieve the...
The Issue: Impacted Welch Allyn products may not meet the Defibrillation Withstand...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Q-Tel. The Q-Tel RMS system is a computer-based cardiac and Recalled by...
The Issue: Impacted Welch Allyn products may not meet the Defibrillation Withstand...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Q-Stress/XScribe. Q-Stress or XScribe is a diagnostic device capable of...
The Issue: Impacted Welch Allyn products may not meet the Defibrillation Withstand...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ELI PC. The ELI PC Service automatically converts resting ECG Recalled by...
The Issue: Impacted Welch Allyn products may not meet the Defibrillation Withstand...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: S4 and patient cable for the S4 Wireless Telemeter with Recalled by WELCH...
The Issue: Impacted Welch Allyn products may not meet the Defibrillation Withstand...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: H12+ and patient cable for the H12+ Holter Recorders with Recalled by WELCH...
The Issue: Impacted Welch Allyn products may not meet the Defibrillation Withstand...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: safeCLINITUBES Blood Sampler Recalled by Radiometer Medical ApS Due to The...
The Issue: The SafeCLINITUBES blood sampler may have insufficient aspiration...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: safeCLINITUBES Blood Sampler Recalled by Radiometer Medical ApS Due to The...
The Issue: The SafeCLINITUBES blood sampler may have insufficient aspiration...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: safeCLINITUBES Blood Sampler Recalled by Radiometer Medical ApS Due to The...
The Issue: The SafeCLINITUBES blood sampler may have insufficient aspiration...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: DR. THAMES - LAP CHOLE Recalled by Applied Medical Resources Corp Due to...
The Issue: There may be a slightly protruding rivet on the distal end of the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Clip Applier Kit Recalled by Applied Medical Resources Corp Due to There may...
The Issue: There may be a slightly protruding rivet on the distal end of the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.