Class 2 Device Recall Medline Convenience kits

• Date Initiated by Firm: March 03, 2025
• Date Posted: April 17, 2025
• Recall Status: Open, Classified
• Recall Number: Z-1611-2025
• Recall Event ID: 96510
• Product Classification: Labor and Delivery Kit - Product Code MLS
• Product: Medline Convenience kits used for various procedures: 1) LABOR AND DELIVERY PACK-LF, Model Number: DYNJ26971L; 2) VAGINAL DELIVERY PACK-LF, Model Number: DYNJ0378319P; 3) VUWC OB PACK, Model Number: DYNJ64017B; 4) OB PROTECTION PACK NO GAUZE, Model Number: DYNJHTLD04A; 5) PACK VAGINAL DELIVERY, Model Number: HM190A; 6) VAGINAL DELIVERY PACK, Model Number: SYNJ10248B; 7) OB PROTECTION PACK NO GAUZE, Model Number: DYNJ84209; 8) VAG DELIVERY PACK-6220, Model Number: DYNJ49542B; 9) FHT VAG DELIVERY PACK, Model Number: DYNJ37124C; 10) VAGINAL DEL PK, Model Number: DYNJ65689; 11) PK,L&D-VAG DEL, Model Number: DYNJ43737D; 12) L&D PACK-LF, Model Number: DYNJ0731657M; 13) VAGINAL DELIVERY PACK-LF, Model Number: DYNJ43604B; 14) VAD ACCESS, Model Number: DYNJ24276C; 15) VAGINAL DELIVERY PACK, Model Number: DYNJ80304; 16) VAGINAL DELIVERY CDS, Model Number: CDS982762I; 17) VAGINAL DELIVERY, Model Number: DYNJ903796C; 18) VAGINAL DELIVERY PACK, Model Number: DYNJ43677D; 19) VAGINAL DELIVERY PACK, Model Number: DYNJ43677D; 20) BR L&D PACK, Model Number: DYNJ47625B; 21) OB PACK, Model Number: DYNJ03387B; 22) OB PROTECTION PACK NO GAUZE, Model Number: DYNJHTLD04A; 23) VAGINAL DELIVERY TRAY, Model Number: MNS7460A; 24) VAGINAL DELIVERY PACK, Model Number: DYNJ23158B; 25) L AND D PACK, Model Number: DYNJHTLD03A; 26) PK,L&D-VAG DEL, Model Number: DYNJ43737D; 27) VAG DELIVERY PACK, Model Number: DYNJ34949; 28) OB PACK, Model Number: DYNJ55835B; 29) VAGINAL DELIVERY PACK, Model Number: DYNJ68778A; 30) OB PACK, Model Number: DYNJ83115; 31) VAGINAL DEL PK, Model Number: DYNJ65689; 32) LDRP-OBSTETRICAL PACK-LF, Model Number: DYNJ64828B; 33) LABOR & DELIVERY PACK, Model Number: DYNJ69433; 34) LABOR & DELIVERY II-LF, Model Number: DYNJS8250; 35) VAGINAL DELIVERY PACK-MARY IMM, Model Number: DYNJ24514G; 36) CUSTOM VAGINAL DELIVERY, Model Number: DYNJ63270C; 37) BHS STANDARD VAGINAL DELIVERY, Model Number: DYNJ80329; 38) OB VAGINAL PACK-LF, Model Number: DYNJ40009D; 39) DELIVERY PACK ME-LF RF, Model Number: DYNJ45589F; 40) VAGINAL DELIVERY PACK-LF, Model Number: DYNJ82620A; 41) VAGINAL DELIVERY, Model Number: DYNJ903796C; 42) DELIVERY PACK, Model Number: DYNJ69964; 43) VAGINAL DELIVERY PACK, Model Number: DYNJ34315D; 44) VAGINAL DELIVERY PACK, Model Number: DYNJ57668A; 45) VAG DELIVERY PACK CHS-LF, Model Number: DYNJ35608K; 46) O.B. PACK-LF, Model Number: DYNJ07520J; 47) OB PROTECTION PACK NO GAUZE, Model Number: DYNJ84209; 48) VAGINAL DELIVERY PACK, Model Number: DYNJ68778A; 49) CUH VAGINAL-LF, Model Number: DYNJC9242C; 50) VAGINAL DELIVERY, Model Number: DYNJ903796C; 51) VAGINAL DELIVERY, Model Number: DYNJ907958; 52) VAG DEL PROCEDURE MCSETX, Model Number: DYNJ908581A; 53) CUH VAGINAL-LF, Model Number: DYNJC9242C; 54) VAGINAL DELIVERY, Model Number: DYNJ903796C; 55) VAGINAL DELIVERY, Model Number: DYNJ907958
• Code Information: 1) DYNJ26971L, UDI-DI: 10198459087158(each), 40198459087159(case), Lot Number: 24IBD872; 2) DYNJ0378319P, UDI-DI: 10198459105722(each), 40198459105723(case), Lot Number: 24IBF374; 3) DYNJ64017B, UDI-DI: 10195327550325(each), 40195327550326(case), Lot Number: 24IBG070; 4) DYNJHTLD04A, UDI-DI: 10193489303346(each), 40193489303347(case), Lot Number: 24IBH288; 5) HM190A, UDI-DI: 10195327305161(each), 40195327305162(case), Lot Number: 24IBH818; 6) SYNJ10248B, UDI-DI: 10193489373387(each), 40193489373388(case), Lot Number: 24IBH820; 7) DYNJ84209, UDI-DI: 10195327342739(each), 40195327342730(case), Lot Number: 24IBH988; 8) DYNJ49542B, UDI-DI: 10195327388072(each), 40195327388073(case), Lot Number: 24IBR452; 9) DYNJ37124C, UDI-DI: 10195327416195(each), 40195327416196(case), Lot Number: 24IBR491; 10) DYNJ65689, UDI-DI: 10193489284836(each), 40193489284837(case), Lot Number: 24IBR570; 11) DYNJ43737D, UDI-DI: 10193489350845(each), 40193489350846(case), Lot Number: 24IBR650; 12) DYNJ0731657M, UDI-DI: 10195327697020(each), 40195327697021(case), Lot Number: 24IBR661; 13) DYNJ43604B, UDI-DI: 10193489997521(each), 40193489997522(case), Lot Number: 24IBR707; 14) DYNJ24276C, UDI-DI: 10884389431184(each), 40884389431185(case), Lot Number: 24IBS408; 15) DYNJ80304, UDI-DI: 10195327022532(each), 40195327022533(case), Lot Number: 24IBS686; 16) CDS982762I, UDI-DI: 10193489942095(each), 40193489942096(case), Lot Number: 24JBB609; 17) DYNJ903796C, UDI-DI: 10195327623371(each), 40195327623372(case), Lot Number: 24JBE762; 18) DYNJ43677D, UDI-DI: 10193489768589(each), 40193489768580(case), Lot Number: 24JBM324; 19) DYNJ43677D, UDI-DI: 10193489768589(each), 40193489768580(case), Lot Number: 24JBM600; 20) DYNJ47625B, UDI-DI: 10889942182589(each), 40889942182580(case), Lot Number: 24JBN320; 21) DYNJ03387B, UDI-DI: 10195327191092(each), 40195327191093(case), Lot Number: 24JBO026; 22) DYNJHTLD04A, UDI-DI: 10193489303346(each), 40193489303347(case), Lot Number: 24JBR630; 23) MNS7460A, UDI-DI: 10653160996392(each), 40653160996393(case), Lot Number: 24JBU227; 24) DYNJ23158B, UDI-DI: 10195327473891(each), 40195327473892(case), Lot Number: 24JBU459; 25) DYNJHTLD03A, UDI-DI: 10193489303353(each), 40193489303354(case), Lot Number: 24JBU555; 26) DYNJ43737D, UDI-DI: 10193489350845(each), 40193489350846(case), Lot Number: 24JBV052; 27) DYNJ34949, UDI-DI: 10884389403358(each), 40884389403359(case), Lot Number: 24JBV802; 28) DYNJ55835B, UDI-DI: 10195327319946(each), 40195327319947(case), Lot Number: 24JBV820; 29) DYNJ68778A, UDI-DI: 10198459035852(each), 40198459035853(case), Lot Number: 24JBV866; 30) DYNJ83115, UDI-DI: 10195327232979(each), 40195327232970(case), Lot Number: 24JBV884; 31) DYNJ65689, UDI-DI: 10193489284836(each), 40193489284837(case), Lot Number: 24JBW792; 32) DYNJ64828B, UDI-DI: 10198459140280(each), 40198459140281(case), Lot Number: 24JBX788; 33) DYNJ69433, UDI-DI: 10193489940985(each), 40193489940986(case), Lot Number: 24JBX797; 34) DYNJS8250, UDI-DI: 10884389349298(each), 40884389349299(case), Lot Number: 24KBA046; 35) DYNJ24514G, UDI-DI: 10193489893656(each), 40193489893657(case), Lot Number: 24KBA388; 36) DYNJ63270C, UDI-DI: 10193489862614(each), 40193489862615(case), Lot Number: 24KBB101; 37) DYNJ80329, UDI-DI: 10195327027193(each), 40195327027194(case), Lot Number: 24KBB586; 38) DYNJ40009D, UDI-DI: 10195327362362(each), 40195327362363(case), Lot Number: 24KBC597; 39) DYNJ45589F, UDI-DI: 10198459125904(each), 40198459125905(case), Lot Number: 24KBC628; 40) DYNJ82620A, UDI-DI: 10198459150081(each), 40198459150082(case), Lot Number: 24KBC810; 41) DYNJ903796C, UDI-DI: 10195327623371(each), 40195327623372(case), Lot Number: 24KBD009; 42) DYNJ69964, UDI-DI: 10195327000660(each), 40195327000661(case), Lot Number: 24KBE397; 43) DYNJ34315D, UDI-DI: 10198459168369(each), 40198459168360(case), Lot Number: 24KBF136; 44) DYNJ57668A, UDI-DI: 10193489795622(each), 40193489795623(case), Lot Number: 24KBG150; 45) DYNJ35608K, UDI-DI: 10195327099022(each), 40195327099023(case), Lot Number: 24KBG823; 46) DYNJ07520J, UDI-DI: 10198459015533(each), 40198459015534(case), Lot Number: 24KBG847; 47) DYNJ84209, UDI-DI: 10195327342739(each), 40195327342730(case), Lot Number: 24KBG879; 48) DYNJ68778A, UDI-DI: 10198459035852(each), 40198459035853(case), Lot Number: 24KBH870; 49) DYNJC9242C, UDI-DI: 10193489568882(each), 40193489568883(case), Lot Number: 24KBL933; 50) DYNJ903796C, UDI-DI: 10195327623371(each), 40195327623372(case), Lot Number: 24KBN086; 51) DYNJ907958, UDI-DI: 10193489949445(each), 40193489949446(case), Lot Number: 24KBQ773; 52) DYNJ908581A, UDI-DI: 10195327594664(each), 40195327594665(case), Lot Number: 24KBU702; 53) DYNJC9242C, UDI-DI: 10193489568882(each), 40193489568883(case), Lot Number: 24LBK538; 54) DYNJ903796C, UDI-DI: 10195327623371(each), 40195327623372(case), Lot Number: 24LBO942; 55) DYNJ907958, UDI-DI: 10193489949445(each), 40193489949446(case), Lot Number: 25ABA840
• Recalling Firm/ Manufacturer: MEDLINE INDUSTRIES, LP - Northfield; 3 Lakes Dr; Northfield IL 60093-2753
• For Additional Information Contact: Haley Barclay; 866-359-1704
• Manufacturer Reason for Recall: There is a potential for open/weak seals on purchased breather pouches used for packaging of select sterile convenience kits.
• FDA Determined Cause: Under Investigation by firm
• Action: An IMMEDIATE ACTION REQUIRED MEDLINE DEVICE RECALL notification letter dated 3/3/25 was sent to customers. REQUIRED ACTION: 1.Immediately check your stock for the affected item number and the affected lot numbers which can be located within the recall portal. 2.Please use the link and the information below to complete your response form. Please list the quantity of affected product you have in inventory on the form. Even if you do not have any affected product in inventory, please complete and submit the response form. 3.Please destroy any affected inventory. Medline will issue credit for the product based upon the quantity and lot numbers identified on the submitted response form The login for completing the response form is: Website link: https://recalls.medline.com Recall Reference #: R-25-050-FG Recall Code: RECALL CODE 4.If you are a distributor, or have resold or transferred this product to another company or individual, you are required by FDA regulations to notify them of this recall communication. Please request that customers document and destroy any affected product, and include your customer s quantities on your response form. If you have any questions, contact the Recall Department at 866-359-1704 or recalls@medline.com.
• Quantity in Commerce: 21935 units
• Distribution: Worldwide distribution - US Nationwide and the countries of Canada, Mexico, Panama, Virgin Islands.
• Total Product Life Cycle: TPLC Device Report

¹ A record in this database is created when a firm initiates a correction or removal action. The record is updated if the FDA identifies a violation and classifies the action as a recall, and it is updated for a final time when the recall is terminated. Learn more about medical device recalls.
² Per FDA policy, recall cause determinations are subject to modification up to the point of termination of the recall.
³ The manufacturer has initiated the recall and not all products have been corrected or removed. This record will be updated as the status changes.