SCISSORS, OR, SHARP/BLUNT, 5.5", STERILE, Item Number DYN... – the items may have weak packaging sea... (2025)
This recall involves packaging or cosmetic issues.
This AI-generated summary is provided for general informational purposes only and is derived from publicly available recall notices. It supplements but does not replace official agency classifications or safety instructions.
Check Your Product
According to the U.S. Food and Drug Administration (FDA)
Product
SCISSORS, OR, SHARP/BLUNT, 5.5", STERILE, Item Number DYND04000
Lot Codes / Batch Numbers
DYND04000, UDI-DI: 10193489191349(each), 20193489191346(case), Lot Number: 2023102590
Products Sold
DYND04000, UDI-DI: 10193489191349(each), 20193489191346(case), Lot Number: 2023102590
A medical device manufacturer is recalling SCISSORS, OR, SHARP/BLUNT, 5.5", STERILE, Item Number DYND04000 due to The items may have weak packaging seals that may result in a breach of sterility if the seal fails and may lead to an increased risk of infection if p. Based on FDA medical device recall database.
Summary derived from FDA notice
Reason for Recall
As stated by FDA
The items may have weak packaging seals that may result in a breach of sterility if the seal fails and may lead to an increased risk of infection if product is utilized.
Recommended Action
Per FDA guidance
An URGENT MEDICAL DEVICE RECALL notification letter dated 11/13/25 was sent to customers. REQUIRED ACTION: 1. Immediately check your stock for the affected item number(s) and the affected lot number(s) listed on the enclosed response form. Quarantine all affected product. Upon completion of the below actions, please destroy affected product. 2. Please complete and return the enclosed response form listing the quantity of affected product you have in inventory. Even if you do not have any affected product in inventory, please complete and return the response form. 3. Your account will receive credit once the response form is submitted, if applicable. 4. If you are a distributor, or have resold or transferred this product to another company or individual, you are required by FDA regulations to notify them of this recall communication. Please request that customers destroy any affected product. You should include your customers quantities on your response form. If you have any questions, contact the Recall Department at 866-359-1704 or recalls@medline.com.
Verify this information on the official source
This page aggregates publicly available data. Always confirm recall details directly with the U.S. Food and Drug Administration (FDA) before taking action.
View official FDA recall noticePage updated: Jan 10, 2026
Important Notice
This page displays information sourced from the U.S. Food and Drug Administration (FDA). IsMyProductRecalled.com aggregates public data for convenience and does not issue recalls. We are not affiliated with any government agency. Always verify recall information with the official source before taking action. This is not medical or legal advice.