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. 2,743 recalls have been distributed to South Carolina in the last 12 months.
Showing 1801–1820 of 28,688 recalls
Recalled Item: Posterior Femoral Augment Recalled by Waldemar Link GmbH & Co. KG (Mfg Site)...
The Issue: The device was delivered with a preassembled Femoral Augment screw that was...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Tibial Augment Recalled by Waldemar Link GmbH & Co. KG (Mfg Site) Due to The...
The Issue: The device was delivered with a preassembled Femoral Augment screw that was...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Enhanced Verify Evaluation Handset (CFN HH90130FA) Recalled by Medtronic...
The Issue: Evaluation handsets may not be able to communicate with the neurostimulator...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Distal Femoral Augment Recalled by Waldemar Link GmbH & Co. KG (Mfg Site)...
The Issue: The device was delivered with a preassembled Femoral Augment screw that was...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: L-Shaped Femoral Augment Recalled by Waldemar Link GmbH & Co. KG (Mfg Site)...
The Issue: The device was delivered with a preassembled Femoral Augment screw that was...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: MAGEC 2 Rod Recalled by Globus Medical, Inc. Due to Devices for the affected...
The Issue: Devices for the affected lot were not assembled according to product...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Biomet 3i Certain-compatible 4.1 mm Milled Ti Abutment Recalled by Preat...
The Issue: Due to manufacturing issues, abutment products were manufactured with screw...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Washer Disinfector Aquadis 56 Recalled by Getinge Disinfection Ab Due to The...
The Issue: The frequency inverter is not programmed by supplier according to...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Washer Disinfector Aquadis 56 Recalled by Getinge Disinfection Ab Due to The...
The Issue: The frequency inverter is not programmed by supplier according to...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: myQA iON Recalled by IBA Dosimetry GmbH Due to Wrong analysis results can...
The Issue: Wrong analysis results can occur if the user creates two structures with the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Philips Brilliance CT Big Bore Recalled by Philips North America Llc Due to...
The Issue: Unintended motion issues related to Interventional Control that may lead to...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Ultrasonic Cleaning Systems Triton 36 Model Number 6003000804 Triton 72...
The Issue: During routine preventative maintenance checks, it was revealed that carbon...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Halyard CHRIST SUTURE KIT. General Procedure Tray Convenience Kit Recalled...
The Issue: An issue with a raw material used to coat some surgical needles that may...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Halyard RAPIDES E-PACK. Cardiovascular Procedure Convenience Kit. Recalled...
The Issue: An issue with a raw material used to coat some surgical needles that may...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Halyard SUTURE PACK CABG. Cardiovascular Procedure Convenience Kit. Recalled...
The Issue: An issue with a raw material used to coat some surgical needles that may...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: 3.0 Liter Disposable Set (4 sets/case). Model Number: 903-00032. The...
The Issue: Potential crack in the female connector located on the Heat...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Hyperthermia Pump Procedure Kit. Model Number: 902-00045. Sterile Recalled...
The Issue: Potential crack in the female connector located on the Heat Exchanger in the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Stratus CS Acute Care cTNI TestPak.IVD test for cardiac troponin Recalled by...
The Issue: Siemens Healthcare Diagnostics Inc., is recalling their Stratus CS Acute...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Straight Inflow/Outflow Patient Line Kit. Model Number: 902-00037. Sterile...
The Issue: Potential crack in the female connector located on the Heat Exchanger in the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Straight Inflow/Bifurcated Outflow Line Kit. Model Number: 902-00038....
The Issue: Potential crack in the female connector located on the Heat Exchanger in the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.