ClearanceBrief
Recall Z-0957-2012 ยท HRX Arthroscope

Ascent Healthcare Solutions

***CAT 375-544-000***STRYKER***Arthroscopic Blade***4.0mm AGGRESSIVE PLUS***Hub Style - Formula***Red/Lt Blue***SAMPLE LATEX-FREE***Made in the USA***Manufacturer: ASCENT HEALTHCARE SOLUTIONS***Lakeland, FL*** Lot number: 200860***Expiration Date: 01/2012. ***CAT 375-554-000***STRYKER***Arthroscopic Blade***5.0mm AGGRESSIVE PLUS***Hub Style - Formula***Red/Lt Blue***SAMPLE LATEX-FREE***Made in t

DateFeb 3, 2012 (initiated Jan 26, 2009)
StatusTerminated
ReasonOn 01/26/2009, Ascent Healthcare Solutions, Lakeland, FL initiated a recall of various models of Dyonics, Stryker, and Linvatech Reprocessed Arthroscopic Shaver Blades. The sterility of the devices may be compromised due to a potential breach in the seal of the Tyvek cover to the plastic tray.
Root causePackaging process control
ActionAscent Healthcare Solutions sent an "URGENT MEDICAL DEVICE VOLUNTARY RECALL" letter dated January 26, 2009 to all affected customers. The letter describes the product, problem, and actions to be taken by the customers. Customers were instructed to examine their inventory, remove and quarantine all affected devices. A Recall Effectiveness Check Form was attached for customers to complete and return via fax to 1-866-325-4760. Contact the firm at (888) 888-3433 ext. 5519 for questions regarding this recall.
Quantity1575 devices
DistributionWorldwide Distribution-USA (nationwide) including the states of AK, AL, AR, AZ, CA, CO, CT, FL, GA, HI, IA, ID, IL, IN, KS, KY, LA, MA, ME, MI, MN, MO, MS, MT, NC, ND, NH, NV, NY, OH, OK, OR, PA, RI, SD, TN, TX, UT, VA, WA, WI, and WY, and the country of Canada.
FDA recordOpen on fda.gov

510(k) clearances named in this recall

K012605REPROCESSED ATHROSCOPICS BURS
Alliance Medical Corp., Nov 7, 2001
K012635REPROCESSED STRYKER ARTHROSCOPIC SHAVERS
Alliance Medical Corp., Nov 7, 2001