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. 2,723 recalls have been distributed to South Carolina in the last 12 months.
Showing 4461–4480 of 28,688 recalls
Recalled Item: Ingenia 1.5T Recalled by Philips North America Llc Due to Patient support...
The Issue: Patient support table floor plate may be incorrectly installed.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: GYROSCAN T10-NT Recalled by Philips North America Llc Due to Patient support...
The Issue: Patient support table floor plate may be incorrectly installed.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Intera 3.0T Quasar Dual Recalled by Philips North America Llc Due to Patient...
The Issue: Patient support table floor plate may be incorrectly installed.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Ingenia 3.0T Recalled by Philips North America Llc Due to Patient support...
The Issue: Patient support table floor plate may be incorrectly installed.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Ingenia Ambition S Recalled by Philips North America Llc Due to Patient...
The Issue: Patient support table floor plate may be incorrectly installed.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Intera 1.5T Master/Nova Recalled by Philips North America Llc Due to Patient...
The Issue: Patient support table floor plate may be incorrectly installed.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Ingenia 3.0T CX Recalled by Philips North America Llc Due to Patient support...
The Issue: Patient support table floor plate may be incorrectly installed.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ATTUNE AFFIXIUM Cementless Fixed Bearing Knee with 3DP Technology Recalled...
The Issue: Product incorrectly labelled.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: OsmoPRO MAX Automated Osmometer- IVD Osmometer for Clinical Use. Uses...
The Issue: System error messages may delay the ability to test patient samples and the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Identity Imprint PS Tibial Tray Size 4: Lot 540287 Recalled by Conformis,...
The Issue: Size 5 Tibial Tray from Lot 508287 was packaged in a Size 4 box from Lot...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: RENASYS EDGE 300ML CANISTER WITH Solidifier- Indicated for patients who...
The Issue: Black particulate matter from the carbon filter component of the canisters...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: RENASYS EDGE 800ML CANISTER WITH Solidifier- Indicated for patients who...
The Issue: Black particulate matter from the carbon filter component of the canisters...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: HDS Traction Boot II Recalled by Baxter Healthcare Corporation Due to Baxter...
The Issue: Baxter Healthcare Corporation is issuing an Urgent Medical Device Recall for...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Galaxy System (specifically GAL-019 Recalled by Noah Medical Due to Due to a...
The Issue: Due to a misaligned calibration of the wired controller that may result in...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: STRATAFIX Spiral MONOCRYL Plus Bidirectional Knotless Tissue Control Device:...
The Issue: Degraded and unusable upon removal from the foil pouch due to exposed...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: POWERSEAL 5 mm Recalled by Olympus Corporation of the Americas Due to Upon...
The Issue: Upon initial activation of the seal function, the POWERSEAL non-conformance...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: POWERSEAL 5 mm Recalled by Olympus Corporation of the Americas Due to Upon...
The Issue: Upon initial activation of the seal function, the POWERSEAL non-conformance...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: POWERSEAL 5 mm Recalled by Olympus Corporation of the Americas Due to Upon...
The Issue: Upon initial activation of the seal function, the POWERSEAL non-conformance...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Tablo Hemodialysis System Recalled by Outset Medical, Inc. Due to...
The Issue: Hemodialysis System, pre and post dialyzer peroxide-cured silicone tubing,...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: CryoValve SG Cryopreserved Pulmonary Human Heart Valve Recalled by Artivion,...
The Issue: The blood cultures performed as part of the organ donation process were...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.