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. 1,670 recalls have been distributed to South Dakota in the last 12 months.
Showing 40781–40800 of 47,632 recalls
Recalled Item: 5/10/12 mm Weck¿ Vista" Universal Cannula Recalled by Teleflex Medical Due...
The Issue: Complaints were received of leakage of insufflation gas through the device,...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: 12mm Weck¿ Vista" Cannula-only Recalled by Teleflex Medical Due to...
The Issue: Complaints were received of leakage of insufflation gas through the device,...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: 5/10 Weck Vista Universal Balloon Open Access Port - Standard Length (70mm)...
The Issue: Complaints of leakage of insufflation gas through the device.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Sutures Recalled by Teleflex Medical Due to The products are being recalled...
The Issue: The products are being recalled because they did not meet minimum needle...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: 5/10/12 Weck¿ Vista" Universal Balloon Open Access Port Long Length...
The Issue: Complaints were received of leakage of insufflation gas through the device,...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: 5/10 mm Weck Vista Optical Bladeless Laparoscopic Access Port Recalled by...
The Issue: Complaints of leakage of insufflation gas through the device.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: 5/10 mm Weck¿ Recalled by Teleflex Medical Due to Complaints were received...
The Issue: Complaints were received of leakage of insufflation gas through the device,...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Weck¿ Vista" Universal Laparoscopic Port Recalled by Teleflex Medical Due to...
The Issue: Complaints were received of leakage of insufflation gas through the device,...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: 5/10 Weck¿ Vista" Universal Balloon Open Access Port - Long Length (100mm)...
The Issue: Complaints were received of leakage of insufflation gas through the device,...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: CAPIO Recalled by Teleflex Medical Due to The product did not meet minimum...
The Issue: The product did not meet minimum and/or average minimum Teleflex resorption...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: 5/10 Weck¿ Vista" Universal Balloon Open Access Port - Standard Length...
The Issue: Complaints were received of leakage of insufflation gas through the device,...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Integra CUSA Excel Disposable Wrench. Catalog Number C5601. The CUSA...
The Issue: Some 23 kHz Torque Wrenches were incorrectly assembled and contained a 36...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: SpaceLabs Arkon Anesthesia Delivery System with Version 2.0 Software...
The Issue: The System may go into a controlled failed state if a series of parameters...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Lupron Depot (Leuprolide Acetate for Depot Suspension) Single Dose...
The Issue: Defective Delivery System: Some Lupron Depot Kits may containin a syringe...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Lupron Depot (Leuprolide Acetate for Depot Suspension) Single Dose...
The Issue: Defective Delivery System: Some Lupron Depot Kits may contain a syringe with...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: LUPRON DEPOT-PED (Leuprolide Acetate for Depot Suspension) Single Dose...
The Issue: Defective Delivery System: Some Lupron Depot Kits may contain a syringe with...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Lupron Depot (leuprolide acetate for depot suspension) Single Dose...
The Issue: Defective Delivery System: Some Lupron Depot Kits may contain a syringe with...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Lupron Depot (Leuprolide Acetate for Depot Suspension) Single Dose...
The Issue: Defective Delivery System: Some Lupron Depot Kits may contain a syringe with...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Halogen Lamp component in RetCam 3 System - Clarity Medical Systems Recalled...
The Issue: One lot of Halogen lamps have the potential to fail sooner than the expected...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Ingenuity Core 128 Recalled by Philips Medical Systems (Cleveland) Inc Due...
The Issue: A customer reported that after upgrading to software version 3.5.5 from...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.