Stryker Endoscopy 26" Vision Elect HDTV Surgical Viewing Monitor, model number 0240030960, Manufactured by Stryker Endoscopy San Jose Intended to be used as a visualization device for events occurring in the sterile field for endoscopic surgical procedures. Recall
Check Your Product
According to the U.S. Food and Drug Administration (FDA)
Product
26" Vision Elect HDTV Surgical Viewing Monitor, model number 0240030960, Manufactured by Stryker Endoscopy San Jose Intended to be used as a visualization device for events occurring in the sterile field for endoscopic surgical procedures.
Brand
Stryker Endoscopy
Lot Codes / Batch Numbers
PER Number(s): 98131, 99085, 101141, 105591, 101235, 101212, 109617, 110104, 110852, 110974, 111006, 111048, 111081, 111105, 111181, 111199, 111202, 111303, 111492, 111562, 111595, 111868, 111912, and 111935
Products Sold
PER Number(s): 98131, 99085,101141,105591,101235,101212, 109617, 110104, 110852,110974,111006,111048,111081,111105, 111181, 111199, 111202, 111303, 111492, 111562, 111595, 111868, 111912, and 111935
Stryker Endoscopy is recalling 26" Vision Elect HDTV Surgical Viewing Monitor, model number 0240030960, Manufactured by Stryker End due to Knob parts stick together, resulting in poor functionality of the knob.. Based on FDA medical device recall database.
Summary derived from FDA notice
Reason for Recall
As stated by FDA
Knob parts stick together, resulting in poor functionality of the knob.
Recommended Action
Per FDA guidance
Urgent: Device Correction letters dated 9/22/2008 were sent to Sales representatives and all accounts. Sales reps were also notified via email. Each Sales Rep was provided rework instructions, a list of affected accounts and serial numbers, and new knobs to install on affected units. Customers were asked to inspect their inventory for the part number, they were informed that their sales rep would be responsible for replacing the rotary knobs on all affected units, and that they should contact their sales rep to schedule the knob replacement.
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 noticeDistribution
As reported by FDA
AL, AZ, AR, CA, CO, CT, DE, FL, GA, HI, ID, IL, IN, IA, KS, KY, LA, MD, MA, MI, MN, MO, MT, NE, NV, NJ, NM, NY, NC, ND, OH, OK, OR, PA, RI, SC, SD, TN, TX, UT, VT, VA, WA, WV, WI, WY, DC
Page updated: Jan 10, 2026