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. 2,349 recalls have been distributed to South Dakota in the last 12 months.
Showing 27481–27500 of 27,558 recalls
Recalled Item: MicroCool Breathable Impervious Gown with Secure Fit Surgical Recalled by...
The Issue: Complaints were received of gowns pilling or balling, linting and abrades,...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Baxter's elastomeric infusion pumps are non-electronic Recalled by Baxter...
The Issue: There are reported incidents of leakage on the INFUSOR and FOLFUSOR pumps at...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Baxter's elastomeric infusion pumps are non-electronic Recalled by Baxter...
The Issue: There are reported incidents of leakage on the INFUSOR and FOLFUSOR pumps at...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Baxter's elastomeric infusion pumps are non-electronic Recalled by Baxter...
The Issue: There are reported incidents of leakage on the INFUSOR and FOLFUSOR pumps at...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Whole Body X--ray Scanner This device is indicated as a Recalled by Toshiba...
The Issue: 1. It has been found that in raw data processing for Go&Return helical...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: OEC IT3000 Recalled by GE OEC Medical Systems, Inc Due to GE Healthcare...
The Issue: GE Healthcare Surgery had discovered that using the Inverted Headset...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Electrode Recalled by Karl Storz Endoscopy America Inc Due to Possible...
The Issue: Possible damage to the sterile packaging (blister tray) of some Karl Storz...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Electrode Recalled by Karl Storz Endoscopy America Inc Due to Possible...
The Issue: Possible damage to the sterile packaging (blister tray) of some Karl Storz...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Electrode Recalled by Karl Storz Endoscopy America Inc Due to Possible...
The Issue: Possible damage to the sterile packaging (blister tray) of some Karl Storz...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Electrode Recalled by Karl Storz Endoscopy America Inc Due to Possible...
The Issue: Possible damage to the sterile packaging (blister tray) of some Karl Storz...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Loop Recalled by Karl Storz Endoscopy America Inc Due to Possible damage to...
The Issue: Possible damage to the sterile packaging (blister tray) of some Karl Storz...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Electrode Recalled by Karl Storz Endoscopy America Inc Due to Possible...
The Issue: Possible damage to the sterile packaging (blister tray) of some Karl Storz...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Electrode Recalled by Karl Storz Endoscopy America Inc Due to Possible...
The Issue: Possible damage to the sterile packaging (blister tray) of some Karl Storz...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Electrode Recalled by Karl Storz Endoscopy America Inc Due to Possible...
The Issue: Possible damage to the sterile packaging (blister tray) of some Karl Storz...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Knife Recalled by Karl Storz Endoscopy America Inc Due to Possible damage to...
The Issue: Possible damage to the sterile packaging (blister tray) of some Karl Storz...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Electrode Recalled by Karl Storz Endoscopy America Inc Due to Possible...
The Issue: Possible damage to the sterile packaging (blister tray) of some Karl Storz...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Loop Recalled by Karl Storz Endoscopy America Inc Due to Possible damage to...
The Issue: Possible damage to the sterile packaging (blister tray) of some Karl Storz...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Electrode Recalled by Karl Storz Endoscopy America Inc Due to Possible...
The Issue: Possible damage to the sterile packaging (blister tray) of some Karl Storz...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Triage TOX Drug Screen Panel Recalled by Alere San Diego, Inc. Due to...
The Issue: Biosite is recalling the Triage TOX Drug Screen kits where the box...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Sunquest Encompass The reporting site is using the Encompass software...
The Issue: Sunquest is recalling the Sunquest Encompass versions 2.4 and later because...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.