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. 2,386 recalls have been distributed to South Dakota in the last 12 months.
Showing 21901–21920 of 27,558 recalls
Recalled Item: NS-3600-B LITE GLOVE 1000/CASE -Bulk Recalled by Covidien LLC Due to Devon...
The Issue: Devon Light Gloves contain splits or holes compromising the sterility
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Delivery/C-Section Recalled by Covidien LLC Due to Devon Light Gloves...
The Issue: Devon Light Gloves contain splits or holes compromising the sterility
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Surgical Kit Sterile-Kits containing the Devon Light Glove Catalog...
The Issue: Devon Light Gloves contain splits or holes compromising the sterility
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Mini-Kits Recalled by Covidien LLC Due to Devon Light Gloves contain splits...
The Issue: Devon Light Gloves contain splits or holes compromising the sterility
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Hysto Pack Recalled by Covidien LLC Due to Devon Light Gloves contain splits...
The Issue: Devon Light Gloves contain splits or holes compromising the sterility
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Major Kit Recalled by Covidien LLC Due to Devon Light Gloves contain splits...
The Issue: Devon Light Gloves contain splits or holes compromising the sterility
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Augmentation Kit Recalled by Covidien LLC Due to Devon Light Gloves contain...
The Issue: Devon Light Gloves contain splits or holes compromising the sterility
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Minor Surgical Kits Recalled by Covidien LLC Due to Devon Light Gloves...
The Issue: Devon Light Gloves contain splits or holes compromising the sterility
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ASC (Breast) Kit Recalled by Covidien LLC Due to Devon Light Gloves contain...
The Issue: Devon Light Gloves contain splits or holes compromising the sterility
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Double Basin Kit Recalled by Covidien LLC Due to Devon Light Gloves contain...
The Issue: Devon Light Gloves contain splits or holes compromising the sterility
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Non Sterile Subassembly: Catalog Number/Description: SA1008 NONSTERILE...
The Issue: Devon Light Gloves contain splits or holes compromising the sterility
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: AXIOM ARISTOS FX Recalled by Siemens Medical Solutions USA, Inc Due to If...
The Issue: If the cable cart and the corrugated hose are unable to move freely, the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Philips Healthcare Ingenuity CT Computed Tomography X-ray system Recalled by...
The Issue: During scans with specific protocol steps, the software unexpectedly sets...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Philips Healthcare Ingenuity Core 128 Computed Tomography X-ray system...
The Issue: During scans with specific protocol steps, the software unexpectedly sets...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: KimVent Turbo-Cleaning Closed Suction System for Adults Recalled by Halyard...
The Issue: The internal blue flapper valve of certain KimVent Turbo-Cleaning Closed...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Philips Healthcare Brilliance 64 Computed Tomography X-ray system Recalled...
The Issue: During scans with specific protocol steps, the software unexpectedly sets...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Philips Healthcare Ingenuity Core Computed Tomography X-ray system Recalled...
The Issue: During scans with specific protocol steps, the software unexpectedly sets...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: SIEMENS Luminos Agile Max Recalled by Siemens Medical Solutions USA, Inc Due...
The Issue: Study and all acquired images deleted when using systems with software...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: SIEMENS Axiom Luminos dRF Max Recalled by Siemens Medical Solutions USA, Inc...
The Issue: Study and all acquired images deleted when using systems with software...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: SIEMENS Uroskop Omnia Max Recalled by Siemens Medical Solutions USA, Inc Due...
The Issue: Study and all acquired images deleted when using systems with software...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.