FDAFDA · Food and drugs·Recall number Z-2705-2024
Medline medical procedure kits labeled as follows: a) ENDO KIT, REF DYK1012268E1
Published August 28, 2024 · Recall initiated: March 22, 2024
Status when published: Ongoing — openFDA updates weekly, so this field may not reflect the current status. Always confirm with the official notice.
What's the hazard
A slight dimensional variation which has the potential for increased difficulty fitting into outer canister.
What to do
Voluntary: Firm initiated · Two or more of the following: Email, Fax, Letter, Press Release, Telephone, Visit
Recall details
- Manufacturer
- MEDLINE INDUSTRIES, LP - Northfield
- Distributor
- Worldwide - US Nationwide and the countries of Panama, Mexico, Canada, Qatar, El Salvador, Oman, Colombia, Singapore.
- Lot
- a) REF DYK1012268E1, UDI/DI 40884389919089 (case), 10884389919088 (unit), Lot Numbers: 22FBU931, 22HBL619, 22JBG192, 22LBH957, 23CBU467, 23FBS319, 23IBT789, 23KMH977
- Risk classification
- Class II
- Area (FDA)
- device
- Country
- United States
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