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. 2,516 recalls have been distributed to South Dakota in the last 12 months.
Showing 7241–7260 of 47,632 recalls
Recalled Item: Brand Name: Guardian 2 System Product Name: Guardian System 2 Recalled by...
The Issue: A software issue where "low" and "terminal" battery alerts did not display...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Atrium Oasis Drain Single W / AC Recalled by Atrium Medical Corporation Due...
The Issue: A sterilization nonconformance prematurely aged the product by 48.3 days,...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Change Healthcare Stratus Imaging PACS 1.4 and Stratus Imaging Share 1.4...
The Issue: Under certain circumstances, information from HL7 messages received by...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Infusomat Administration Sets as listed below: 362031 Infusomat Space Pump...
The Issue: In affected products, the tubing outer diameter may vary in size or the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ADLT BLOOD CULTURE COLLECT KIT Recalled by MEDLINE INDUSTRIES, LP -...
The Issue: This recall is being issued due to items within the kit have expired prior...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: PERIPHERAL BLOOD CULTURE DRAW Recalled by MEDLINE INDUSTRIES, LP -...
The Issue: This recall is being issued due to items within the kit have expired prior...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: BLOOD CULTURE KIT Recalled by MEDLINE INDUSTRIES, LP - Northfield Due to...
The Issue: This recall is being issued due to items within the kit have expired prior...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: 24 BLOOD CULTURE KIT Recalled by MEDLINE INDUSTRIES, LP - Northfield Due to...
The Issue: This recall is being issued due to items within the kit have expired prior...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: CENTRAL LINE BLOOD CULTURE DRA Recalled by MEDLINE INDUSTRIES, LP -...
The Issue: This recall is being issued due to items within the kit have expired prior...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: LEADER brand Dry Eye Relief (Polyethylene Glycol 400 Recalled by Cardinal...
The Issue: Non-Sterility: FDA found insanitary conditions and positive bacterial test...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: LEADER brand Eye Irritation Relief (Polyvinyl alcohol 0.5% Recalled by...
The Issue: Non-Sterility: FDA found insanitary conditions and positive bacterial test...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: LEADER brand Lubricant Eye Drops (Carboxymethylcellulose Sodium Recalled by...
The Issue: Non-Sterility: FDA found insanitary conditions and positive bacterial test...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Polyvinyl Alcohol 1.4% Lubricating Eye Drops Recalled by The Harvard Drug...
The Issue: Non-Sterility: FDA found insanitary conditions and positive bacterial test...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: LEADER brand Dry Eye Relief (Carboxymethylcellulose Sodium Recalled by...
The Issue: Non-Sterility: FDA found insanitary conditions and positive bacterial test...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: LEADER brand Lubricant Eye Drops (Propylene Glycol Recalled by Cardinal...
The Issue: Non-Sterility: FDA found insanitary conditions and positive bacterial test...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: LEADER brand Lubricant Eye Drops (Carboxymethylcellulose Sodium Recalled by...
The Issue: Non-Sterility: FDA found insanitary conditions and positive bacterial test...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Lubricating Tears Eye Drops (Dextran/Hypromellose) Recalled by The Harvard...
The Issue: Non-Sterility: FDA found insanitary conditions and positive bacterial test...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Acrobat-i Vacuum Positioner System Recalled by Maquet Cardiovascular, LLC...
The Issue: The Positioner Arm may not tighten or lock during normal use.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: The 4Kscore Test Recalled by BioReference Health, LLC Due to Mathematical...
The Issue: Mathematical modeling of the 4Kscore with and without DRE information was...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Snapshot NIR Recalled by KENT IMAGING, INC. Due to Tissue oxygenation...
The Issue: Tissue oxygenation measurement system touchscreens may be unresponsive,...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.