Oasis Medical Inc Premier Edge MVR 19g Microsurgical Knife, Item PE-3519 Recall
Check Your Product
According to the U.S. Food and Drug Administration (FDA)
Product
Premier Edge MVR 19g Microsurgical Knife, Item PE-3519
Brand
Oasis Medical Inc
Lot Codes / Batch Numbers
Lot #'s DK0107W, DK1106G, DK1106R
Products Sold
Lot #'s DK0107W, DK1106G, DK1106R
Oasis Medical Inc is recalling Premier Edge MVR 19g Microsurgical Knife, Item PE-3519 due to This voluntary recall has been initiated due to the product puncturing the packing during rough handling. Once the packaging is damaged, the product i. Based on FDA medical device recall database.
Summary derived from FDA notice
Reason for Recall
As stated by FDA
This voluntary recall has been initiated due to the product puncturing the packing during rough handling. Once the packaging is damaged, the product is no longer sterile as labeled.
Recommended Action
Per FDA guidance
Notification of the recall sent to distributors and users. The 06/08/07 letter requests customers to notify down to the user level. Included in the Recall Notification Letter are instructions: "In addition, if you may have further distributed this product, please identify your customers and notify them at once ofthis product recall. Your notification to your customers may be enhanced by including a copy of this recall notification letter. This recall should be carried out to the user level. Your assistance is appreciated and necessary to prevent any inconvenience."
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