Product Recalls in North Carolina
Product recalls affecting North Carolina — including food, drugs, consumer products, medical devices, and vehicles distributed to North Carolina. RecallDetector monitors distribution data from the FDA, USDA, CPSC, and NHTSA to show you which recalls are relevant to your area. 1,920 recalls have been distributed to North Carolina in the last 12 months.
Showing 23621–23640 of 29,737 recalls
Recalled Item: 3/16 in. Curved Trocar with Wound Drain Curved Trocar with Recalled by...
The Issue: Stryker Instruments is voluntarily recalling the CBCII Wound Drains and...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: 1/4 in. Round Drain with Trocar Curved Trocar with Wound Recalled by Stryker...
The Issue: Stryker Instruments is voluntarily recalling the CBCII Wound Drains and...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Iamin Moist Dressing and the Iamin Hydrating Gel: intended to Recalled by...
The Issue: The labeling for the Iamin family of medical devices (e.g. printed and...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Diamedix Is-CMV IgG Test Kit Recalled by Diamedix Corporation Due to Product...
The Issue: Product contained an incorrect substrate.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: CSA Medical truFreeze Console- Cryosurgical Unit Cryogenic Surgical Device...
The Issue: TruFreeze Console caused a higher rate of liquid nitrogen (cryogen) to be...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Universal Charger Product Usage: The Stryker Universal Battery Charger is...
The Issue: The Stryker Universal Battery Charger is not transmitting usage data to the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: TIGERPAW System II Recalled by Laax, Inc. Due to Increase of field reports...
The Issue: Increase of field reports involving issues with the TIGERPAW System II...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Light Sheer Desire Diode Laser System with XC Handpiece Accessory options....
The Issue: Device software treatment preset parameters for the XC treatment handpiece...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: TIGERPAW System II Recalled by Laax, Inc. Due to Increase of field reports...
The Issue: Increase of field reports involving issues with the TIGERPAW System II...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Synthes Small Battery Drive (SBD) Oscillating Saw Attachment Part Number:...
The Issue: The potential exists for the Oscillating Saw Attachment to disengage from...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Hamilton-G5 Ventilators with software versions V2.40/2.41 Catalog numbers...
The Issue: Customer reports that the ventilator display can freeze. Ventilation...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ADVIA Chemistry Lipase Reagent Recalled by Siemens Healthcare Diagnostics,...
The Issue: Siemens internal investigation confirmed that current contamination...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Homocysteine test system - Homocysteine Reagent. 05385415190 Recalled by...
The Issue: Customers complained about under-recovery of non-Roche controls and...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Covidien Trellis 6 and Trellis 8 Peripheral Infusion Systems Recalled by...
The Issue: Medtronic is conducting a voluntary recall of all former Covidien Trellis 6...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Philips DigitalDiagnost Release 4.0.3 Recalled by Philips Electronics North...
The Issue: The system is designed to emit a beep upon termination of an exposure....
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Edwards Lifesciences Fem-Flex II Femoral Arterial Cannula 8 Recalled by...
The Issue: Edwards Lifesciences is recalling Fem-Flex II Pediatric Femoral Arterial...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Sedecal SA Mobile Diagnost w DR x-ray system Recalled by Sedecal USA, Inc....
The Issue: Due to a software defect, the system may sporadically apply the default x...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Axis-Shield Liquid Stable (LS) 2-Part HOMOCYSTEINE REAGENT Recalled by...
The Issue: Deterioration in performance of the Liquid Stable (LS) 2-Part HOMOCYSTEINE...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Carter-Thomason II Port Closure System Recalled by CooperSurgical, Inc. Due...
The Issue: The pad printing around the suture entry holes on the 15mm Suture Guide...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Artis Q/ Q zen systems Recalled by Siemens Medical Solutions USA, Inc Due to...
The Issue: potential issue with the Artis Q/ Q zen systems where it is possible that an...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.