FDA Recall Open, Classified

Medline procedure packs containing Shenli syringes, labeled as follows: 1) ANGIOGRAPHY DRAPE PACK, Pack Number 00-398281J ; 2) ANGIOGRAPHY DRAPE PACK, Pack Number 00-398650AG; 3) ANGIOGRAPHY DRAPE PACK, Pack Number 00-398650AI; 4) ANGIOGRAPHY DRAPE PK, Pack Number 00-398712S ; 5) CATH LAB PACK , Pack Number 00-398725AM; 6) ANGIOGRAPHY DRAPE PACK, Pack Number 00-399360K ; 7) ANGIOGRAPHY DRAPE PACK, Pack Number 00-399734N ; 8) ANGIOGRAPHY DRAPE PACK, Pack Number 00-399983Q ; 9) ANGIOGRAPHY DRAPE PACK, Pack Number 00-399983R ; 10) ANGIOGRAPHY DRAPE PACK, Pack Number 00-400065K ; 11) ANGIO PROCEDURE PACK, Pack Number 00-400069F ; 12) ANGIOGRAPHY DRAPE PACK PTCA , Pack Number 00-400123AC; 13) ANGIOGRAPHY DRAPE PACK PTCA , Pack Number 00-400123AD; 14) ANGIO PROCEDURE PACK, Pack Number 00-400290D ; 15) ANGIOGRAPHY DRAPE PACK, Pack Number 00-400305Q ; 16) MOUNT SINAI HOSPITAL-ANGIO PK , Pack Number 00-400763F ; 17) ANGIOGRAPHY DRAPE PACK-LF , Pack Number 00-400863J ; 18) ANGIOGRAPHY DRAPE , Pack Number 00-400932O ; 19) ANGIOGRAPHY DRAPE PACK, Pack Number 00-401030S ; 20) ANGIOGRAPHY DRAPE PACK, Pack Number 00-401178D ; 21) ANGIO PROCEDURE PACK, Pack Number 00-401189I ; 22) ANGIOGRAPHY DRAPE PACK, Pack Number 00-401226K ; 23) ANGIOGRAPHY DRP PK PEDI CATH, Pack Number 00-401318L ; 24) ANGIOGRAPHY DRP PK PEDI CATH, Pack Number 00-401318M ; 25) ANGIOGRAPHY DRAPE PACK, Pack Number 00-401327Y ; 26) CORONARY ANGIO PACK-LF, Pack Number 00-401594Q ; 27) ANGIOGRAPHY DRAPE PACK, Pack Number 00-401620J ; 28) ANGIO PROCEDURE PACK, Pack Number 00-401824AA; 29) CATH LAB PACK-LF, Pack Number 00-HCT055P ; 30) CATH ACCESSORY PACK , Pack Number 0M-CP31433G; 31) CATH ACCESSORY PACK , Pack Number 0M-CP31433I; 32) ANGIO PACK, Pack Number 0M-CP31933C; 33) ANGIOGRAPHY PACK-LF , Pack Number 0M-CP32357I; 34) ANGIOGRAPHY PACK-LF , Pack Number 0M-CP32357J; 35) ANTERIOR CERVICAL CDS-LF, Pack Number CDS982292D ; 36) CABG 1, Pack Number CDS983663J ; 37) CATH CDS, Pack Number CDS984141I ; 38) ENDO AAA, Pack Number CDS984264I ; 39) ANGIOGRAPHY OR, Pack Number CDS984944C ; 40) ACCESS CATHETER , Pack Number CDS985507F ; 41) ARTHROSCOPY SHOULDER, Pack Number CDS985509F ; 42) SYMPHONY 5FR CATHETER KIT , Pack Number CTK-5K ; 43) SYMPHONY MAX 6FR CATHETER KIT , Pack Number CTK-6K ; 44) NEURO ANGIO PACK, Pack Number DYNDA1431A; 45) ANGIOGRAPHY PACK-LF , Pack Number DYNJ0048560A ; 46) SJ CATH LAB PACK-LF , Pack Number DYNJ0101429L ; 47) SJ CATH LAB PACK-LF , Pack Number DYNJ0101429N ; 48) ANGIO TRAY-LF , Pack Number DYNJ0131200P ; 49) ANGIOGRAM , Pack Number DYNJ0149444J ; 50) ANGIOGRAM , Pack Number DYNJ0149444K ; 51) ANGIOGRAM , Pack Number DYNJ0149444M ; 52) EP LAB DEVICE PACK-LF , Pack Number DYNJ0160556D ; 53) PED CATH PROCEDURE CHILD PK-LF, Pack Number DYNJ0161241F ; 54) no name , Pack Number DYNJ0161241F ; 55) ANGIO PACK-LF , Pack Number DYNJ0165039M ; 56) ANGIO PACK-LF , Pack Number DYNJ0165039N ; 57) ANGIOGRAPHY DRAPE PACK-LF , Pack Number DYNJ0194989AF; 58) ANGIOGRAPHY DRAPE PACK-LF , Pack Number DYNJ0194989AG; 59) VASCULAR ANGIO PACK-LF, Pack Number DYNJ0201109AG; 60) ANGIOGRAPHY TRAY-LF , Pack Number DYNJ0220880V ; 61) ANGIOGRAPHY DRAPE PACK-LF , Pack Number DYNJ0241256L ; 62) ANGIO PACK-LF , Pack Number DYNJ0281048I ; 63) ANGIOGRAPHY PACK-LF , Pack Number DYNJ0290716L ; 64) ANGIO PROCEDURE PACK-LF , Pack Number DYNJ0298504AG; 65) ANGIOGRAPHIC PACK-LF, Pack Number DYNJ0337491C ; 66) ARTERIOGRAM PACK-LF , Pack Number DYNJ0362293D ; 67) CATH LAB PACK-LF, Pack Number DYNJ0362352M ; 68) CATH PACK-LF, Pack Number DYNJ0367643Q ; 69) ANGIOGRAPHY DRAPE PACK-LF , Pack Number DYNJ0370415I ; 70) CATH LAB PACK-LF, Pack Number DYNJ0371696O ; 71) ANGIOGRAPHY PACK-LF , Pack Number DYNJ0372025G ; 72) OR ANGIOGRAPHY PACK-LF, Pack Number DYNJ0373098K ; 73) OR ANGIOGRAPHY PACK-LF, Pack Number DYNJ0373098L ; 74) OR ANGIOGRAPHY PACK-LF, Pack Number DYNJ0373098M ; 75) ANGIOGRAPHY DRAPE PACK-LF , Pack Number DYNJ

Recall: Z-2627-2024 · Initiated April 8, 2024

Recall

Recall Number: Z-2627-2024
Event Number: 94582
Firm: MEDLINE INDUSTRIES, LP Northfield
FEI Number: 1417592
Product Code: OEQ
Status: Open, Classified
Root Cause: Nonconforming Material/Component
Initiated: April 8, 2024
Posted: August 27, 2024
Address: 3 Lakes Dr, Northfield, IL, 60093-2753

Description

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.

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.

Distribution

Worldwide distribution.

Quantity

1,679,067 units in total