Medline C Section Pack (Medline) – syringe quality alert (2025)
Check Your Product
According to the U.S. Food and Drug Administration (FDA)
Product
Medline procedure kits labeled as: 1) C SECTION, Pack Number DYNJ909098
Brand
MEDLINE INDUSTRIES, LP Northfield
Lot Codes / Batch Numbers
1) 10195327273132 (each) 40195327273133 (case), Lot Number 23GBK039Z
Products Sold
1) 10195327273132 (each) 40195327273133 (case), Lot Number 23GBK039Z
MEDLINE INDUSTRIES, LP Northfield is recalling Medline procedure kits labeled as: 1) C SECTION, Pack Number DYNJ909098 due to Medical convenience kits contain plastic syringes affected by the FDA Safety Alert issued on March 19, 2024. Leaks, breakage, and/other quality issues. 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 02/11/2025 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 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. This is an expansion of 94581
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