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Class 2 Device Recall DePuy Synthes - Food and Drug …
- https://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfRes/res.cfm?ID=182662
- DePuy Synthes issued Urgent Medical Device Removal letter dated July 21, 2020 stating reason for recall, health risk and action to take: Please take the following actions: 1. Immediately examine...
2022 Medical Device Recalls | FDA
- https://www.fda.gov/medical-devices/medical-device-recalls/2022-medical-device-recalls
- 2021 Medical Device Recalls Subscribe to Medical Device Safety and Recalls Sign up to receive email updates on medical device recalls, safety communications, and other …
Class 2 Device Recall Synthes Electric Pen Drive (EPD) …
- https://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfRES/res.cfm?id=132629
- Class 2 Device Recall Synthes Electric Pen Drive (EPD) System. Synthes Electric Pen Drive (EPD) System, The Synthes Electric Pen Drive is indicated for screw …
Class 3 Device Recall DePuy Synthes SYNMESH - Food …
- https://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfres/res.cfm?id=184002
- Recall Number: Z-0403-2021: Recall Event ID: 86545: 510(K)Number: K983766 K003275 Product Classification: Spinal vertebral body replacement device - …
Class 2 Device Recall Synthes XRL Medium TrialCentral …
- https://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfRES/res.cfm?id=126770
- Action Required: Synthes has record that your facility has the product(s) subject to this recall. Synthes asks that you review your inventory and immediately …
Class 2 Device Recall Synthes Radial Head Prosthesis …
- https://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfRES/res.cfm?id=152471
- Synthes (USA) Products LLC 1301 Goshen Pkwy West Chester PA 19380-5986: Manufacturer Reason for Recall: There is the possibility that the radial stem may …
Cleaning & Sterilization Guidelines | DePuy Synthes - J&J MedTech
- https://www.jnjmedtech.com/en-US/service-details/cleaning-sterilization-guidelines/depuy-synthes
- The proper processing of devices is paramount to ensuring patient safety. Since cleaning and sterilization instructions vary among device manufacturers, health care facilities must …
Medical Device Recalls | FDA
- https://www.fda.gov/medical-devices/medical-device-safety/medical-device-recalls
- If you wish to find information on a recall, or a correction or removal action that has not yet been classified, you can search the Medical Device Recalls Database. …
DePuy Orthopaedics | DePuy Synthes
- https://www.jnjmedtech.com/en-US/companies/depuy-synthes
- DePuy Synthes solutions, in specialties including joint reconstruction, trauma, craniomaxillofacial, spinal surgery and sports medicine, in addition to the VELYS™ Digital …
Recall of Device Recall DePuy Synthes Titanium Recon …
- https://medicaldevices.icij.org/events/usa-device-recall-depuy-synthes-titanium-recon-screws
- International Medical Devices Database Events Recall of Device Recall DePuy Synthes Titanium Recon Screws According to U.S. Food and Drug Administration, this recall …
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