Anesthesia Circuit Peds Kit (Medline) – Syringe Quality Issues (2024)
Check Your Product
According to the U.S. Food and Drug Administration (FDA)
Product
Medline procedural kits labeled as: 1) ANESTHESIA CIRCUIT PEDS-LF, Pack Number DYNJAA0327F; 2) ANESTHESIA CIRCUIT PEDS-LF, Pack Number DYNJAA0327G
Brand
MEDLINE INDUSTRIES, LP Northfield
Lot Codes / Batch Numbers
DYNJAA0327F, Lot Number 20LBV329, DYNJAA0327G, Lot Number 21FBM358, DYNJAA0327G, Lot Number 22CBY412, DYNJAA0327G, Lot Number 22GBZ157, DYNJAA0327G, Lot Number 22JBR268, DYNJAA0327G, Lot Number 23BBL309, DYNJAA0327G, Lot Number 23HBU238, DYNJAA0327G, Lot Number 23KBB605, DYNJAA0327G, Lot Number 24CBJ211
Products Sold
DYNJAA0327F , Lot Number 20LBV329 ; DYNJAA0327G , Lot Number 21FBM358 ; DYNJAA0327G , Lot Number 22CBY412 ; DYNJAA0327G , Lot Number 22GBZ157 ; DYNJAA0327G , Lot Number 22JBR268 ; DYNJAA0327G , Lot Number 23BBL309 ; DYNJAA0327G , Lot Number 23HBU238 ; DYNJAA0327G , Lot Number 23KBB605 ; DYNJAA0327G , Lot Number 24CBJ211 ;
MEDLINE INDUSTRIES, LP Northfield is recalling Medline procedural kits labeled as: 1) ANESTHESIA CIRCUIT PEDS-LF, Pack Number DYNJAA0327F; 2) AN due to Medical convenience kits contain plastic syringes affected by the FDA Safety Alert issued on March 19, 2024. Leaks, breakage, and/ other quality issue. Based on FDA medical device recall database.
Summary derived from FDA notice
Reason for Recall
As stated by FDA
Medical convenience kits contain plastic syringes affected by the FDA Safety Alert issued on March 19, 2024. Leaks, breakage, and/ other quality issues have been identified that may pose a risk to patient health.
Recommended Action
Per FDA guidance
Medline Industries LP issued a recall notice to its consignees on 04/08/2024 via letter delivered via USPS and email. The notice explained the issue, provided a link to for information pertaining to the risk involved https://www.fda.gov/medical-devices/safety-communications/update-evaluating-plastic-syringes-made-china-potential-device-failures-fda-safety-communication) and request the syringes within the convenience be discarded, except for circumstances where no alternative syringes are readily available. If these syringes must be used, closely monitor for leaks, breakage, and any other problems, and report any quality issues to Medline and the FDA. Distributors were directed to notify their customers. The firm issued a second recall notice (an expansion) on 05/02/2024 using the same methods.
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