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. 2,339 recalls have been distributed to South Dakota in the last 12 months.
Showing 33081–33100 of 47,632 recalls
Recalled Item: Vaxcel PICC with PASV Catheter Kit under the following labels: 1) 3F...
The Issue: PICC catheters that contain valve(s) manufactured prior to July 15, 2014...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Vaxcel PICC with PASV MST-60 Kit under the following labels: 1) 3F Recalled...
The Issue: PICC catheters that contain valve(s) manufactured prior to July 15, 2014...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Xcela Hybrid PICC with PASV Valve Technology Recalled by Navilyst Medical,...
The Issue: PICC catheters that contain valve(s) manufactured prior to July 15, 2014...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: BioFlo Hybrid PICC with ENDEXO and PASV Valve Technology Recalled by...
The Issue: PICC catheters that contain valve(s) manufactured prior to July 15, 2014...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: BioFlo PICC with ENDEXO and PASV Valve Technology Recalled by Navilyst...
The Issue: PICC catheters that contain valve(s) manufactured prior to July 15, 2014...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Xcela Hybrid PICC with PASV Valve Technology Recalled by Navilyst Medical,...
The Issue: PICC catheters that contain valve(s) manufactured prior to July 15, 2014...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: BioFlo Hybrid PICC with ENDEXO and PASV Valve Technology Recalled by...
The Issue: PICC catheters that contain valve(s) manufactured prior to July 15, 2014...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: CDI Blood Parameter Monitoring System 500 Cardiopulmonary bypass on-line...
The Issue: Specific CDI¿ Blood Parameter Monitoring System 500 devices are being...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: BioFlo PICC with ENDEXO and PASV Valve Technology Recalled by Navilyst...
The Issue: PICC catheters that contain valve(s) manufactured prior to July 15, 2014...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Vaxcel PICC with PASV MST-30 Kit under the following labels: 1) 4F Recalled...
The Issue: PICC catheters that contain valve(s) manufactured prior to July 15, 2014...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Xcela PICC with PASV Valve Technology Recalled by Navilyst Medical, Inc., an...
The Issue: PICC catheters that contain valve(s) manufactured prior to July 15, 2014...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Vaxcel PICC with PASV Intermediate Safety MST Kit under the Recalled by...
The Issue: PICC catheters that contain valve(s) manufactured prior to July 15, 2014...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Artis One Recalled by Siemens Medical Solutions USA, Inc Due to After...
The Issue: After importing segmentation results of the left atrium created on the Artis...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Miltex Premium Grade Self-Lock Chisel Blade Handle Recalled by Integra York...
The Issue: One lot of self-lock chisel blade handles have a wider slot that holds the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Integra 3 Recalled by RESEARCH INSTRUMENTS LTD - SITE B Due to The units...
The Issue: The units have been fitted with a potentially faulty power supply cable.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Integra Meshed Dermal Regeneration Template 5 cmx 5 cm (2 Recalled by...
The Issue: Integra's post QA release review of historical product release test results...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Ceftriaxone Sodium (Sterile) USP active pharmaceutical ingredient Recalled...
The Issue: CGMP Deviations: active pharmaceutical ingredient intermediates failed...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Ceftriaxone for Injection USP Recalled by Lupin Pharmaceuticals Inc. Due to...
The Issue: CGMP Deviations: finished products manufactured using active pharmaceutical...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Ceftriaxone for Injection USP Recalled by Lupin Pharmaceuticals Inc. Due to...
The Issue: CGMP Deviations: finished products manufactured using active pharmaceutical...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Ceftriaxone for Injection USP Recalled by Lupin Pharmaceuticals Inc. Due to...
The Issue: CGMP Deviations: finished products manufactured using active pharmaceutical...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.