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FDA Medical Device Recalls (openFDA)

MEDLINE INDUSTRIES, LP - Northfield: Medline Convenience kits labeled as: 1) STERILE LIDOCAINE SYRINGE PACK, Pack Number DYNDM1076A ; 2) PEDIATRIC EP PACK , Pack Number DYNJ45158A ; 3) CARDIAC MINOR-LF, Pack Number DYNJ51939; 4) CARDIAC MINOR SURGICOUNT PACK , Pack Number DYNJ56573; 5) PEDIATRIC EP PACKMHS, Pack Number DYNJ58876A

Recall number
Z-2986-2024
Recalling firm
MEDLINE INDUSTRIES, LP - Northfield
Product
Medline Convenience kits labeled as: 1) STERILE LIDOCAINE SYRINGE PACK, Pack Number DYNDM1076A ; 2) PEDIATRIC EP PACK , Pack Number DYNJ45158A ; 3) CARDIAC MINOR-LF, Pack Number DYNJ51939; 4) CARDIAC MINOR SURGICOUNT PACK , Pack Number DYNJ56573; 5) PEDIATRIC EP PACKMHS, Pack Number DYNJ58876A
Status
Open, Classified
Initiated
2024-04-08
Posted
2024-09-06
Terminated
not on file
Reason
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.
Root cause
Under Investigation by firm
Action
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 these 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.
Quantity
not on file
Distribution
Worldwide distribution.
Lot, serial or model codes
DYNDM1076A . Lot Number 19CBP748 ; DYNDM1076A . Lot Number 19DBH317 ; DYNDM1076A . Lot Number 19FBT944 ; DYNJ45158A . Lot Number 21KBK059 ; DYNJ45158A . Lot Number 21LBB289 ; DYNJ45158A . Lot Number 19ABZ159 ; DYNJ45158A . Lot Number 22DBS953 ; DYNJ45158A . Lot Number 22GBC899 ; DYNJ45158A . Lot Number 22GBE801 ; DYNJ45158A . Lot Number 19FBG969 ; DYNJ45158A . Lot Number 19FBM779 ; DYNJ45158A . Lot Number 19GBS210 ; DYNJ45158A . Lot Number 19HBS882 ; DYNJ45158A . Lot Number 19IBN282 ; DYNJ45158A . Lot Number 19JBB002 ; DYNJ45158A . Lot Number 23ABR333 ; DYNJ45158A . Lot Number 23CBK931 ; DYNJ45158A . Lot Number 23HBJ279 ; DYNJ45158A . Lot Number 23IBF733 ; DYNJ45158A . Lot Number 20HBR669 ; DYNJ45158A . Lot Number 20HBX586 ; DYNJ45158A . Lot Number 20LBZ104 ; DYNJ45158A . Lot Number 21EBP316 ; DYNJ51939. Lot Number 22CBA086 ; DYNJ51939. Lot Number 19ABY439 ; DYNJ51939. Lot Number 22OBI663 ; DYNJ51939. Lot Number 19HBH583 ; DYNJ51939. Lot Number 19IBU567 ; DYNJ51939. Lot Number 19JBW741 ; DYNJ51939. Lot Number 19JBX646 ; DYNJ51939. Lot Number 20FBT320 ; DYNJ51939. Lot Number 20LBF765 ; DYNJ51939. Lot Number 20LBK574 ; DYNJ56573. Lot Number 19ABN855 ; DYNJ56573. Lot Number 19CBF516 ; DYNJ56573. Lot Number 19EBQ417 ; DYNJ56573. Lot Number 19HBP237 ; DYNJ56573. Lot Number 19UBC593 ; DYNJ56573. Lot Number 19VBA937 ; DYNJ56573. Lot Number 19KBB135 ; DYNJ58876A . Lot Number 20HBW903 ; DYNJ58876A . Lot Number 20IBJ399 ; DYNJ58876A . Lot Number 20IBM299
510(k) numbers
not on file
PMA numbers
not on file
Product code
OGD
Firm FEI
1417592
Firm city
Northfield
Firm state
IL
Firm country
not on file

Where this comes from

Register
FDA Medical Device Recalls (openFDA)
Publisher
U.S. Food and Drug Administration (openFDA)
File
device-recall-0001-of-0001.json.zip
sha256
b87518bfe2e8
Size
288210821 bytes
Published
2026-09-28
Read
2026-09-29T08:25:23.626Z
Source file
Source file retained · verify
Refresh due
2026-10-06

Unless otherwise noted, the content, data, documentation, code, and related materials on openFDA is public domain and made available with a Creative Commons CC0 1.0 Universal dedication.

Cite as

FDA Medical Device Recalls (openFDA) (U.S. Food and Drug Administration (openFDA)), device-recall-0001-of-0001.json.zip, sha256 b87518bfe2e8, published 2026-09-28

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