Ascent Healthcare Solutions ***CAT 7205345***DYONICS***Arthroscopic Blade***4.5mm INCISOR PLUS, 13cm long***Fits Power/EP-1 Motor Drives***Violet***SAMPLE LATEX-FREE***Made in the USA***Manufacturer: ASCENT HEALTHCARE SOLUTIONS***Lakeland, FL*** Lot number: 197940***Expiration Date: 12/2011. Reprocessed arthroscopic shavers are indicated for use in orthopedic surgical procedures of the joints, jaw or sinuses where cutting and removal of soft and hard tissue or bone is needed in patients requiring orthopedic surgery. Recall
Check Your Product
According to the U.S. Food and Drug Administration (FDA)
Product
***CAT 7205345***DYONICS***Arthroscopic Blade***4.5mm INCISOR PLUS, 13cm long***Fits Power/EP-1 Motor Drives***Violet***SAMPLE LATEX-FREE***Made in the USA***Manufacturer: ASCENT HEALTHCARE SOLUTIONS***Lakeland, FL*** Lot number: 197940***Expiration Date: 12/2011. Reprocessed arthroscopic shavers are indicated for use in orthopedic surgical procedures of the joints, jaw or sinuses where cutting and removal of soft and hard tissue or bone is needed in patients requiring orthopedic surgery.
Brand
Ascent Healthcare Solutions
Lot Codes / Batch Numbers
Lot number: 197940
Products Sold
Lot number: 197940
Ascent Healthcare Solutions is recalling ***CAT 7205345***DYONICS***Arthroscopic Blade***4.5mm INCISOR PLUS, 13cm long***Fits Power/EP-1 Moto due to On 01/26/2009, Ascent Healthcare Solutions, Lakeland, FL initiated a recall of various models of Dyonics, Stryker, and Linvatech Reprocessed Arthrosco. Based on FDA medical device recall database.
Summary derived from FDA notice
Reason for Recall
As stated by FDA
On 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.
Recommended Action
Per FDA guidance
Ascent 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.
Verify this information on the official source
For complete details and official instructions, check the U.S. Food and Drug Administration (FDA) directly.
View official FDA recall noticePage updated: Jan 10, 2026