Stryker Endoscopy Stryker Endoscopy PrepStrap Shoulder Sleeve, Model Number 3910900200, Manufactured by Stryker Endoscopy, San Jose, CA Recall
Check Your Product
According to the U.S. Food and Drug Administration (FDA)
Product
Stryker Endoscopy PrepStrap Shoulder Sleeve, Model Number 3910900200, Manufactured by Stryker Endoscopy, San Jose, CA
Brand
Stryker Endoscopy
Lot Codes / Batch Numbers
lot numbers EN0001, EN0002.
Products Sold
lot numbers EN0001, EN0002.
Stryker Endoscopy is recalling Stryker Endoscopy PrepStrap Shoulder Sleeve, Model Number 3910900200, Manufactured by Stryker Endosc due to Latex-- Certain lots of Product contain undeclared latex.. Based on FDA medical device recall database.
Summary derived from FDA notice
Reason for Recall
As stated by FDA
Latex-- Certain lots of Product contain undeclared latex.
Recommended Action
Per FDA guidance
An Urgent: Device Removal notice, dated 7/27/2009 was sent to the sole distributor, Stryker Orthopaedics in New Jersey. The distributor will execute the sub-recall. The firm intends to scrap all returned product at that facility, who will provide a record of disposition. The distributor will notify consignees via a mail packet that will be sent via FedEx overnight mail. Consignees will be instructed to return all product to the distributor, with credit provided per policy.
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