Stryker Instruments Div. of Stryker Corporation Telescopic Uncoated (Push Button), Product No. SHK TSPL. The product is a Bovie pencil that is 75 inches long compressed, with a telescoping shaft. UDI GTIN 37613327466332 Recall
Check Your Product
According to the U.S. Food and Drug Administration (FDA)
Product
Telescopic Uncoated (Push Button), Product No. SHK TSPL. The product is a Bovie pencil that is 75 inches long compressed, with a telescoping shaft. UDI GTIN 37613327466332
Brand
Stryker Instruments Div. of Stryker Corporation
Lot Codes / Batch Numbers
1922042, 1924003, 1929040, 1929048
Products Sold
1922042, 1924003, 1929040, 1929048
Stryker Instruments Div. of Stryker Corporation is recalling Telescopic Uncoated (Push Button), Product No. SHK TSPL. The product is a Bovie pencil that is 75 i due to Hairline fractures in a component could allow electrical current to arc out of the device, resulting in a burn to the patient and/or user.. Based on FDA medical device recall database.
Summary derived from FDA notice
Reason for Recall
As stated by FDA
Hairline fractures in a component could allow electrical current to arc out of the device, resulting in a burn to the patient and/or user.
Recommended Action
Per FDA guidance
On January 13, 2020, the firm informed customers of the recall via Urgent Medical Device Recall Notification letters. Customers were advised to take the following actions: 1. Immediately check all stock areas and/or operating room storage for affected products. Quarantine and discontinue use of any recalled Stryker SafeAir Smoke Evacuation Pencils or LINA Telescopic Smoke Pencils. 2. Complete the Business Reply Form (BRF) to confirm receipt of Notification and identify how many affected items are currently in your inventory. Please complete and return the BRF even if you dont have any affected product on hand. Return the completed BRF via fax to 8665212762 or email to kara.spath@stryker.com. 3. If you have further distributed this product, please forward the notification to all affected locations. 4. If the BRF for your facility indicates that recalled product is currently on hand, a shipping label will be provided which should be used to return recalled product. Upon receipt of the recalled product, a credit will be applied to your account.
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