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. 2,652 recalls have been distributed to South Carolina in the last 12 months.

51,854 total recalls
2,652 in last 12 months

Showing 1482114840 of 28,688 recalls

Medical DeviceDecember 14, 2018· Bayer Medical Care, Inc.

Recalled Item: MAVIG Portegra or Portegra2 Overhead Counterpoise System (OCS) used in...

The Issue: If the head mount knob is not properly tightened and the operator directly...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceDecember 13, 2018· Arrow International Inc

Recalled Item: Arrow PICC powered by Arrow VPS Precision Stylet Product Code:CDC-44052-VPS2...

The Issue: Kits labeled as containing a 40 cm PICC may contain a 50 cm PICC, and kits...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceDecember 13, 2018· Arrow International Inc

Recalled Item: Arrow PICC powered by Arrow VPS Precision Stylet Product Code:CDC-45052-VPS2...

The Issue: Kits labeled as containing a 40 cm PICC may contain a 50 cm PICC, and kits...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceDecember 13, 2018· Elekta, Inc.

Recalled Item: MOSAIQ¿ Oncology Information System and Sequencer MOSAIQ is an oncology...

The Issue: There is a potential that Wedge IDs were not included in the DICOM RT PLAN...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceDecember 12, 2018· Applied Medical Resources Corp

Recalled Item: GelPOINT Path Transanal Procedural Pack with Epix Electrosurgical L-Hook...

The Issue: Unintentional shifting of the tip insulation of the firm's electrosurgical...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceDecember 12, 2018· Applied Medical Resources Corp

Recalled Item: Epix Electrosurgical Probes with Smoke Evacuation Recalled by Applied...

The Issue: Unintentional shifting of the tip insulation of the firm's electrosurgical...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceDecember 12, 2018· Siemens Healthcare Diagnostics, Inc.

Recalled Item: Dimension Vista 1500 Recalled by Siemens Healthcare Diagnostics, Inc. Due to...

The Issue: When the Millipore Water Purification Module Progard Pretreatment Packs are...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceDecember 12, 2018· Siemens Healthcare Diagnostics, Inc.

Recalled Item: Dimension Vista 500 Recalled by Siemens Healthcare Diagnostics, Inc. Due to...

The Issue: When the Millipore Water Purification Module Progard Pretreatment Packs are...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceDecember 12, 2018· Ion Beam Applications S.A.

Recalled Item: Proteus 235 Product Usage: The Proton Therapy System - Proteus Recalled by...

The Issue: There is a risk of detachment of the Compact Gantry Rolling Floor.

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceDecember 11, 2018· Baxter Healthcare Corporation

Recalled Item: Kaguya Automated Peritoneal Dialysis System Product Usage: It is intended...

The Issue: Potential for the software on Automated PD System cyclers which can cause...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceDecember 11, 2018· Baxter Healthcare Corporation

Recalled Item: AMIA Automated Peritoneal Dialysis System Product Usage: It is intended...

The Issue: Potential for the software on Automated PD System cyclers which can cause...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceDecember 11, 2018· Ortho-Clinical Diagnostics

Recalled Item: VITROS Chemistry Products VALP Reagent Pack. For in vitro diagnostic...

The Issue: Negative bias results when using VITROS VALP Reagent, GEN 25.

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceDecember 11, 2018· Kimberly-Clark Corporation

Recalled Item: U by Kotex¿ Sleek¿ Recalled by Kimberly-Clark Corporation Due to Potential...

The Issue: Potential for tampon to come apart upon removal.

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceDecember 11, 2018· Kimberly-Clark Corporation

Recalled Item: U by Kotex¿ Sleek¿ Recalled by Kimberly-Clark Corporation Due to Potential...

The Issue: Potential for tampon to come apart upon removal.

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceDecember 11, 2018· Kimberly-Clark Corporation

Recalled Item: U by Kotex¿ Sleek¿ Recalled by Kimberly-Clark Corporation Due to Potential...

The Issue: Potential for tampon to come apart upon removal.

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceDecember 11, 2018· Kimberly-Clark Corporation

Recalled Item: U by Kotex¿ Sleek¿ Recalled by Kimberly-Clark Corporation Due to Potential...

The Issue: Potential for tampon to come apart upon removal.

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceDecember 10, 2018· ProSun International, LLC

Recalled Item: ProSun Onyx 32 Sli Intensive (12 minutes) tanning bed Recalled by ProSun...

The Issue: ProSun International LLC discovered discrepancies in their Quality Control...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceDecember 10, 2018· ProSun International, LLC

Recalled Item: ProSun V3 42 Xlc(160w)(10 minutes) tanning bed Recalled by ProSun...

The Issue: ProSun International LLC discovered discrepancies in their Quality Control...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceDecember 10, 2018· Signature Orthopedics Pty Limited

Recalled Item: Genius Knee Cemented Tibial Component Product Usage: Knee replacement...

The Issue: Product mix up

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceDecember 10, 2018· Signature Orthopedics Pty Limited

Recalled Item: Genius Knee Cemented CR Femoral Component Product Usage: Knee replacement...

The Issue: Product mix up

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing