FDA Medical devices recall ·

Medline custom medical procedure kits labeled as: 1) ENSEMBLE RACHIS-LF recall

Recall number
Z-0792-2025
Date
(initiated November 21, 2024)
Company / brand
Medline Industries, LP
3 Lakes Dr, Northfield, IL, United States
Category
Medical devices › Class II
Classification
Class II
Status
Ongoing
Units affected
2664 units
Hazard tags
Sterility Microbial contamination
Initiated by
Voluntary: Firm initiated

Read the official FDA notice ↗

Product

Medline custom medical procedure kits labeled as: 1) ENSEMBLE RACHIS-LF, REF DYNJ47568B; 2) UROLOGY ROBOTIC, REF DYNJ55555D; 3) KIT,SPINE LH, REF DYNJ906448A.

Why was it recalled?

Custom convenience kits are being recall because the contain non-sterile Codman Surgical Patties & Surgical Strips, which have the potential for endotoxin contamination.

What should you do?

FDA enforcement reports do not list a consumer remedy. Check the product codes below against what you have; if it matches, stop using it and follow the instructions in the firm's or FDA's official notice, or contact the company. If you have health concerns, contact your healthcare provider.

Product codes & lot numbers

1) REF DYNJ47568B, UDI/DI 10193489846058 (EA) 40193489846059 (CS), Lot Numbers: 21EBP877, 21EBP891, 21GBW057, 21GBW059, 21KBG927, 21WBA306, 22ABO417, 22EBE351, 22FBX502, 22FBY332, 22IBJ001, 22LBA177, 23ABD998, 23BBE825, 23CBI861, 23EBO916, 23FBQ324, 23GBN118, 23IBL993, 23JBT331, 23LBC938, 24BBG081, 24BBN421, 24EBC753, 24FBM377, 24HBR212, 24HBS302; 2) REF DYNJ55555D, UDI/DI 23HBQ656; 3) REF DYNJ906448A, UDI/DI 20LBO883, 20WBE707, 21CBS664, 21EBG271.

Distribution

Worldwide distribution - US Nationwide and the countries of UAE, and Canada.

What does Class II mean?

Class II means use of or exposure to the product may cause temporary or medically reversible adverse health consequences, or the probability of serious harm is remote.

Source: FDA (medical devices), recall Z-0792-2025. Official notice. Republished from public data; RecallFlag is not affiliated with the FDA.