ClearanceBrief
Recall Z-2413-2019 ยท HRX Arthroscope

Stryker GmbH

Endotrac ECTR Push Blade, Catalog Number 2053-1 The EPF system is designed for the treatment of plantar fasciosis. The EPF system is a minimally invasive surgical technique for chronic plantar fasciitis (fasciosis). The EGR system is designed for the treatment of gastrocnemius equinus.

DateJul 25, 2019
StatusTerminated
ReasonThe seal integrity of the sterile bag containing the kits may be compromised.
Root causePackaging
ActionThe firm, Stryker, sent an "UPDATE URGENT MEDICAL DEVICE RECALL" notification letters dated 7/25/19 were to its customers. The letter described the product, problem and actions to be taken. The customers were instructed to do the following: 1. Please inform users of this Urgent Medical Device Recall and forward this notice to all those individuals who need to be aware within your organization. 2. Immediately check all stock areas and/or operating room storage to determine if any devices from the affected product list are at your facility. A response is required, even though you may not have
Quantity476
DistributionUS Nationwide Distribution
FDA recordOpen on fda.gov

510(k) clearances named in this recall

K940230ENDOSCOPIC MORTONS NEUROMA INSTRUMENTS
Instratek, Inc., Dec 12, 1994