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. 2,521 recalls have been distributed to South Dakota in the last 12 months.
Showing 6461–6480 of 27,558 recalls
Recalled Item: Intelli-C Recalled by NRT X-RAY A/S Due to There is a potential that the...
The Issue: There is a potential that the drive shaft in the detector up/down (IDE)...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: HeartSine Recalled by HeartSine Technologies Ltd Due to Single use battery...
The Issue: Single use battery and electrode cartridge may be rendered inoperable due to...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: FILMARRAY Gastrointestinal (GI) Panel (Part No.: RFIT-ASY-0104 &...
The Issue: The firm has identified an increased risk of obtaining false positive...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Incisive CT for Brazil SKD-Computed Tomography X-Ray System Model: 728146...
The Issue: Metal mounting box on the rotating scanner on rotor (heat exchanger box)...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Incisive CT-Computed Tomography X-Ray System Model: 728143 Recalled by...
The Issue: Metal mounting box on the rotating scanner on rotor (heat exchanger box)...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Incisive CT Power (China)-Computed Tomography X-Ray System Model: 728148...
The Issue: Metal mounting box on the rotating scanner on rotor (heat exchanger box)...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Incisive CT Plus-Computed Tomography X-Ray System Model: 728149 Recalled by...
The Issue: Metal mounting box on the rotating scanner on rotor (heat exchanger box)...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Ventralight ST w Echo PS 4.5" Circle A low profile Recalled by Davol, Inc....
The Issue: Balloon may not inflate as intended. If the balloon does not inflate during...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Ventralight ST w EchoPS 4"x6" Ellipse- A low profile Recalled by Davol, Inc....
The Issue: Balloon may not inflate as intended. If the balloon does not inflate during...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Ventralight ST 4.5" Circle with Echo PS- A low profile Recalled by Davol,...
The Issue: Balloon may not inflate as intended. If the balloon does not inflate during...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Ventralight ST 4" x 6" Ellipse with Echo PS Catalog Number: 5955460 Recalled...
The Issue: Balloon may not inflate as intended. If the balloon does not inflate during...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: SteriPack Sterile Polyester Spun Swabs (25 units/Pack)- Intended for sample...
The Issue: Fails Post-Sterilization Sterile Swabs Cantilever (Bend) Testing and may be...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: LINK SymphoKnee System L-Shaped Femoral Augment Recalled by Linkbio Corp....
The Issue: Contains the incorrect implant in the packaging. The packaging incorrectly...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Xpert Xpress Strep A Recalled by Cepheid Due to pipettes packaged in Strep A...
The Issue: pipettes packaged in Strep A test may fail to dispense an adequate sample...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Xpert Xpress Strep A Recalled by Cepheid Due to pipettes packaged in Strep A...
The Issue: pipettes packaged in Strep A test may fail to dispense an adequate sample...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: AVNS ambIT System - PIB/PCA W 2.5in Cath Recalled by Avanos Medical, Inc....
The Issue: Some of the ambIT kits were potentially distributed without an air in-line...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Alinity i Anti-TPO Reagent Kit Recalled by Abbott Ireland Limited Due to Due...
The Issue: Due to a manufacturing fill volume error, Alinity i Anti-TPO Reagent...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: SMMT ambIT Kit Basic Filter Luer Cass Recalled by Avanos Medical, Inc. Due...
The Issue: Some of the ambIT kits were potentially distributed without an air in-line...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ambIT Cassette Filter Male Luer Recalled by Avanos Medical, Inc. Due to Some...
The Issue: Some of the ambIT kits were potentially distributed without an air in-line...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: SMMT ambIT Reusable Program - Luer Cass Recalled by Avanos Medical, Inc. Due...
The Issue: Some of the ambIT kits were potentially distributed without an air in-line...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.