Medline Industries, LP: Medical Device Recall in 2025 - (Recall #: Z-0886-2026)

Updated on March 25, 2026.

See the recall detail below. You can also see other recalls from the same firm in 2025.

Data Source: FDA.
Product Description:

MEDLINE PERFUSION SYRINGE, REF: DYNJ39223C

Product Classification:

Class II

Date Initiated: October 27, 2025
Date Posted: December 17, 2025
Recall Number: Z-0886-2026
Event ID: 97968
Reason for Recall:

Medline Industries, LP is issuing a recall for specific item(s) and lot(s) of Medline Kits containing BD Luer Tip Caps. BD has issued a recall of their Luer Tip Caps after confirming through internal testing that certain BD Luer Tip Cap trays failed routine biocompatibility testing. Although the tip cap covers a small surface area of the syringe and does not come in direct contact with patients, there is the potential that the failure of a biocompatibility test may have varying consequences ranging from no harm or clinical impact to potential for sensitization, irritation, pyrogenicity, acute systemic toxicity or hemolysis depending on the nature and duration of contact with the syringe.

Status: Ongoing
Product Quantity: 15 units
Code Information:

UDI/DI 10193489621532 (each) 40193489621533 (case), Lot Number 25FMJ081

Distribution Pattern:

US Nationwide distribution in the state of CA.

Voluntary or Mandated:

Voluntary: Firm initiated