Product Recalls in South Carolina
Product recalls affecting South Carolina — including food, drugs, consumer products, medical devices, and vehicles distributed to South Carolina. RecallDetector monitors distribution data from the FDA, USDA, CPSC, and NHTSA to show you which recalls are relevant to your area. 2,727 recalls have been distributed to South Carolina in the last 12 months.
Showing 3701–3720 of 28,688 recalls
Recalled Item: Brand Name: Perfusor Space Product Name: Perfusor Space Syringe Pump...
The Issue: Perfusor Space Syringe Pump's instructions for use previously identified...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Brand Name: Perfusor Space Product Name: Perfusor PCA Syringe Pump Recalled...
The Issue: Perfusor Space Syringe Pump's instructions for use previously identified...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Brand Name: Perfusor Space Product Name: PERFUSOR SPACE ACM-KIT...
The Issue: Perfusor Space Syringe Pump's instructions for use previously identified...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Brand Name: Perfusor Space Product Name: Perfusor Space Infusion Pump...
The Issue: Perfusor Space Syringe Pump's instructions for use previously identified...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Brand Name: Perfusor Space Product Name: Perfusor Space Syringe Pump...
The Issue: Perfusor Space Syringe Pump's instructions for use previously identified...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Nitro Glide Knee Walker-offers users recovering from a below-the-knee injury...
The Issue: The tiller separates from the base/front caster assembly. If the knee walker...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Nitro Glide Knee Walker-offers users recovering from a below-the-knee injury...
The Issue: The tiller separates from the base/front caster assembly. If the knee walker...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Hookup Model/Catalog Number: 2-8-540CAS Product Description: Hookups provide...
The Issue: IFU for hookup were incorrectly within hookup IFUs and online system, Hookup...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Hookup Model/Catalog Number: 2-8-540 Product Description: Hookups provide...
The Issue: IFU for hookup were incorrectly within hookup IFUs and online system, Hookup...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Hookup Model/Catalog Number: 2-8-540HAN Product Description: Hookups provide...
The Issue: IFU for hookup were incorrectly within hookup IFUs and online system, Hookup...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Hookup Model/Catalog Number: DSD-110-HU0163 Product Description: Hookups...
The Issue: IFU for hookup were incorrectly within hookup IFUs and online system, Hookup...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Horizon X-Ray Bone Densitometer (DXA) Models: Horizon-A Recalled by Hologic...
The Issue: Non-conformance pertains to electromagnetic compatibility requirements...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Autotome RX 20mm CUT WIRE Cannulating Sphincterotome Recalled by Boston...
The Issue: Foreign material may be present on the enclosed section of the cutting wire...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: BAUSCH+LOMB Recalled by Synergetics Inc Due to Sterilization certificates...
The Issue: Sterilization certificates could not be validated by the supplier
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: BAUSCH+LOMB Recalled by Synergetics Inc Due to Sterilization certificates...
The Issue: Sterilization certificates could not be validated by the supplier
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: BAUSCH+LOMB Recalled by Synergetics Inc Due to Sterilization certificates...
The Issue: Sterilization certificates could not be validated by the supplier
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: BAUSCH+LOMB Recalled by Synergetics Inc Due to Sterilization certificates...
The Issue: Sterilization certificates could not be validated by the supplier
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Foam Protective Pouches Recalled by Medical Action Industries, Inc. 306 Due...
The Issue: The protective pouches were identified to have been improperly labeled with...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Various Merit Medical convenience kits that contain recalled Jiangsu Shenli...
The Issue: Medical convenience kits contain plastic syringes affected by the FDA Safety...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Various Merit Medical convenience kits that contain recalled Jiangsu Shenli...
The Issue: Medical convenience kits contain plastic syringes affected by the FDA Safety...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.