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. 1,913 recalls have been distributed to North Carolina in the last 12 months.
Showing 24381–24400 of 29,737 recalls
Recalled Item: PKG Recalled by Stryker Endoscopy Due to Stryker Endoscopy is recalling...
The Issue: Stryker Endoscopy is recalling Laparoscopic manual instruments and...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: PKG Recalled by Stryker Endoscopy Due to The parameters provided in the...
The Issue: The parameters provided in the Laparoscopic Manual Instruments Instructions...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: PKG Recalled by Stryker Endoscopy Due to The parameters provided in the...
The Issue: The parameters provided in the Laparoscopic Manual Instruments Instructions...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: PKG Recalled by Stryker Endoscopy Due to The parameters provided in the...
The Issue: The parameters provided in the Laparoscopic Manual Instruments Instructions...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: PKG Recalled by Stryker Endoscopy Due to The parameters provided in the...
The Issue: The parameters provided in the Laparoscopic Manual Instruments Instructions...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: PKG Recalled by Stryker Endoscopy Due to The parameters provided in the...
The Issue: The parameters provided in the Laparoscopic Manual Instruments Instructions...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Synthes Small Electric Drive (SED) Recalled by The Anspach Effort, Inc. Due...
The Issue: May operate solely in reverse mode, not operate in reverse mode when...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Biograph mCT X-4R Recalled by Siemens Medical Solutions USA Inc. Due to...
The Issue: Possibility for system display freeze during CT interventional procedures.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Biograph mCT Flow Edge-4R Recalled by Siemens Medical Solutions USA Inc. Due...
The Issue: Possibility for system display freeze during CT interventional procedures.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Biograph mCT S(64)-4R Recalled by Siemens Medical Solutions USA Inc. Due to...
The Issue: Possibility for system display freeze during CT interventional procedures.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Biograph mCT Flow 40-4R Recalled by Siemens Medical Solutions USA Inc. Due...
The Issue: Possibility for system display freeze during CT interventional procedures.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ABX PENTRA Reagent Container Recalled by Horiba Instruments, Inc dba Horiba...
The Issue: HORIBA Medical is recalling the ABX PENTRA 400 Reagent Container because...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: FLUTTER Percussor respiratory device Recalled by Aptalis Pharmatech Inc. Due...
The Issue: Customer notification that the device may be difficult to open or close.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Biograph mCT S(40)-4R Recalled by Siemens Medical Solutions USA Inc. Due to...
The Issue: Possibility for system display freeze during CT interventional procedures.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Oxoid Legionella BCYE Growth Supplement packaged in packs of 10-100ml...
The Issue: Use of the product could result in inadequate recovery of Legionella...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: I.M. Hole Locator Instrument. Orthopedic manual surgical instrument. The IM...
The Issue: Use of excessive force when impacting may lead to intra-operative femoral...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: BrightView model number: 882478 BrightView X model number: 882480 BrightView...
The Issue: Unintended detector and gantry movement due to software issues.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Syngo.plaza Recalled by Siemens Medical Solutions USA, Inc Due to Printouts...
The Issue: Printouts may be printed in incorrect anatomical size when using syngo.plaza...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Solitaire-C Cervical Spacer System a) 14-531593 Drill/Awl Sleeve b)...
The Issue: A design deficiency was discovered whereby the Drill/Awl Sleeve and...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Alcon Single-Use Curved Jewelers/Iris Bipolar Forceps Sterile RX Recalled by...
The Issue: The product is sold and labeled as EO sterilized, however the units were not...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.