Product Recalls in New Hampshire
Product recalls affecting New Hampshire — including food, drugs, consumer products, medical devices, and vehicles distributed to New Hampshire. RecallDetector monitors distribution data from the FDA, USDA, CPSC, and NHTSA to show you which recalls are relevant to your area. 2,540 recalls have been distributed to New Hampshire in the last 12 months.
Showing 8021–8040 of 27,899 recalls
Recalled Item: Hilal Embolization Microcoil Recalled by Cook Incorporated Due to The...
The Issue: The loading cartridges included with these devices may contain a small,...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: DJO EMPOWR 3D Knee (Right) 10mm Tibial Insert Recalled by Encore Medical, LP...
The Issue: A right, size 8, knee tibial insert package may include a mispackaged, left...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Optiflux 200NRe Dialyzer Finished Assy. Recalled by Fresenius Medical Care...
The Issue: Dialyzers were distributed after being exposed to cold temperatures which...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: PROFEMUR PLASMA Z CLASSIC STEM SIZE 7 STANDARD SHORT NECK Recalled by...
The Issue: One manufacturing lot is missing the plasma-spray coating in the proximal...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: illumina Model NextSeq 550 Dx Recalled by Illumina, Inc. Due to...
The Issue: cybersecurity vulnerability
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: illumina Model: MiSeq Dx illumina Model: Recalled by Illumina, Inc. Due to...
The Issue: cybersecurity vulnerability
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: STORZ KARL STORZ-ENDOSKOPE CMOS Video Cysto-Urethroscope Recalled by Karl...
The Issue: The endoscope may experience a loss of image when activating monopolar...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: NIM Vital Patient Interface 4.0 (P/N: NIM4CPB1) NIM with Software version...
The Issue: Software anomaly was identified.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Ratcheting Screwdriver Handle Recalled by Tornier, Inc Due to The device is...
The Issue: The device is unable to meet sterilization requirements when sterilized per...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: NIM Vital Console 4.0 (P/N: NIM4CM01) NIM with Software version 1.3.2...
The Issue: Software anomaly was identified.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Adult Cap-ONE Biteblock The cap-ONE Biteblock is intended Recalled by Nihon...
The Issue: Due to products being shipped/distributed to customers after the products...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: NIM EMG Endotracheal Tube Recalled by Medtronic Xomed, Inc. Due to The firm...
The Issue: The firm received reports of events related to airway obstruction while...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: NIM CONTACT EMG Endotracheal Tube Recalled by Medtronic Xomed, Inc. Due to...
The Issue: The firm received reports of events related to airway obstruction while...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: NIM EMG Endotracheal Tube Recalled by Medtronic Xomed, Inc. Due to The firm...
The Issue: The firm received reports of events related to airway obstruction while...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: INTERGARD Woven Vascular Graft is a woven polyester graft coated Recalled by...
The Issue: Mislabeled: Product labeled as Intergard Woven Straight graft , D: 8 mm, L:...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Centricity Radiology RA600 Recalled by GE Healthcare, LLC Due to Potential...
The Issue: Potential for Distance and Area measurements to display inaccurate...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Centricity Universal Viewer Zero Footprint Client Recalled by GE Healthcare,...
The Issue: Potential for Distance and Area measurements to display inaccurate...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Centricity Enterprise Web Recalled by GE Healthcare, LLC Due to Potential...
The Issue: Potential for Distance and Area measurements to display inaccurate...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Centricity Cardiology CA1000 Recalled by GE Healthcare, LLC Due to Potential...
The Issue: Potential for Distance and Area measurements to display inaccurate...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Centricity PACS RA1000 Recalled by GE Healthcare, LLC Due to Potential for...
The Issue: Potential for Distance and Area measurements to display inaccurate...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.