Medline Industries, LP recalls Medline convenience kits: ABD PACK DYNJ81673B BARIATRIC DYNJ902515K BARIATRI…
Reason for recall
Kits contain recalled lot of Ferndale Laboratories MASTISOL Liquid Adhesive. Butyrate tubing may crack during actuation and render product unusable for application.
Affected product
Check your device
Enter a lot, serial, REF, or UDI number from your device's label to check it against this recall's listed codes.
Affected products & lots
- Medline convenience kits: ABD PACK DYNJ81673B BARIATRIC DYNJ902515K BARIATRIC + DYNJ904119O BARIATRIC CDS CDS983883J BWNBORO LAP CHOLE PACK-LF DYNJ32836B CCSB KARIN JWIRE LUMPECTOMY DYNJ910459B CHRISTUS CHILDRENS LAP CHOLE DYNJ61165G CUH MINOR PACK-LF DYNJ60095B FREE FLAP CUSTOM PACK B DYNJ82736B FREE NIPPLE GRAFT DYNJ911160B GEN MINOR DYNJ900906L GEN SURG LAPAROSCOPY PACK DYNJ55248F GEN SURG MINOR PACK DYNJ69142F GENERAL LAP DYNJ61475A DYNJT3759 GENERAL LAP PACK DYNJ61515I DYNJT4452 GENERAL LAP PACK-LF DYNJ37208D GENERAL LAPAROSCOPY DYNJ905870G GENERAL LAPAROSCOPY PACK DYNJ17443T DYNJ45263B DYNJT4504 LAP CHOLE DYNJ45664D DYNJ912005 LAP CHOLE PACK DYNJ81695B LAP CHOLE PACK-LF DYNJ0614113C DYNJ0618369V LAP CHOLE PROCEDURE-LF CDS981184D LAP CHOLE RFD DYNJ906302F LAP CHOLE SURGICOUNT DYNJ45531G LAP CHOLE TOTE DYNJ908339F LAP GASTRIC BYPASS CDS CDS860146M LAP GASTRIC PACK DYNJ62065A LAP HERNIA RFD DYNJ906301F LAP PACK DYNJ38871J DYNJ51389A LAPAROSCOPIC CDS920082AC LAPAROSCOPIC PACK DYNJ52605K LAPAROSCOPIC PACK-LF PHS41736G LAPAROSCOPY PACK DYNJT8313 LAPAROSCOPY PACK-LF DYNJ02309D DYNJ0551175T LAPAROSCOPY UM RF DYNJ902324D LAPAROSCOPY-LF DYNJ903241B LAPAROTOMY PACK-LF DYNJ21091O LARGE ABDOMINAL PACK-LF PHS41737D LEX GENERAL LAPAROSCOPY DYNJ900969K MINOR GENERAL PACK DYNJT3884 MINOR PACK-LF DYNJ0105608I MINOR PK DYNJ61335D MINOR PROCEDURE CDS CDS981793G PEDIATRIC MOSES DYNJ58864B PK, GEN-LAPAROSCOPY DYNJ53837B RMC GENERAL LAPAROSCOPIC DYNJ907087C ROBOTIC GENERAL DYNJ906861D SM-GENERAL LAP PACK-LF DYNJ0780078W SMJ GENERAL ABDOMINAL PACK-LF DYNJ25765Q UOFL HOSP GENERAL LAPAROSCOPYDYNJ909321AUDI-DI 10195327494728185 affected lots26AMA776DYNJ902515K1019532766260825KBO749DYNJ904119O1019845907315126ABB89926ABI225
+177 more
26ABJ235CDS983883J1019845942979825KBK403DYNJ32836B1019532703736925LMF151DYNJ910459B1019845947740926AML096DYNJ61165G1019845938670125LBO68326ABE316DYNJ60095B1019845941337725KBB96025LBO686DYNJ82736B1019845903890725LMG794DYNJ911160B1019845939800126AMB749DYNJ900906L1019845940852626AMG179DYNJ55248F1019532763348625KBA350DYNJ69142F1019845947849925LMF407DYNJ61475A1019532760579725JBT649DYNJT37591019845935103725KBJ720DYNJ61515I1019845954299225KBI633DYNJT44521019845946067825JBR785DYNJ37208D1019532743418225LBJ032DYNJ905870G1019845939459125JBP62325LBR135DYNJ17443T1019532769297125KBJ329DYNJ45263B1019348985239425KBH088DYNJT45041019845945670125LMI354DYNJ45664D1019348989851425KBB002DYNJ9120051019845959712125KBT433DYNJ81695B1019845902345325LMJ938DYNJ0614113C1019845935253925KBC852DYNJ0618369V1088994282659926BBC627CDS981184D1019348932481526AMG257DYNJ906302F1019845941985025KBG656DYNJ45531G1019532700603725JBR41325LBN71926BBD403DYNJ908339F1019845940955425KBM957CDS860146M1019532722454725KBK35926ABG74726ABQ780DYNJ62065A1019348927347225LMH990DYNJ906301F1019845941984325LBA148DYNJ38871J1019845924021825LMJ264DYNJ51389A1088994288122225LBR750CDS920082AC1019845923732425KBR576DYNJ52605K1019845925478925LMG367PHS41736G1019845943874525LMG005DYNJT83131019845969715926CBD042DYNJ02309D1019845913443225LBP128DYNJ0551175T1019845953341925KBE001DYNJ902324D1019845912568325KBQ907DYNJ903241B1019348981898726ABF331DYNJ21091O1019845948518325KBA31326CBD177PHS41737D1019845943875225LMG512DYNJ900969K1019845945231426ABG612DYNJT38841019845936684025JBX326DYNJ0105608I1019845953325925KBA34425KBM30625LBE190DYNJ61335D1019532712858625KBA763CDS981793G1019845949368325KBT360DYNJ58864B1019845934696525LBP018DYNJ53837B1019348920973025LBP490DYNJ907087C1019845920130126AMA102DYNJ906861D1019845929370226AMC100DYNJ0780078W1019532763392925JME84525LMK134DYNJ25765Q1019845960367925LMG846DYNJ909321A1019532754562825KBT731
What the firm is doing
Firm began notifying consignees on 4/27/2026. Customers were instructed to request stickers to over-label affected convenience kits with a warning label. Warning label indicates for user to remove the affected component and replace it with product from supply. No kits are to be returned.
DistributionShow detailsHide
US Nationwide distribution. OUS distribution pending.
Use of the product may cause temporary or medically reversible adverse health consequences.
Sources & references
- FDA enforcement recordOfficial FDA database entry for Z-2422-2026
- FDA device classification · FDEOfficial FDA classification for this device type
- CFR regulation · 21 CFR 876.1500The federal regulation governing this device
- FDA recall announcementSearch FDA.gov for the official press announcement
- Find Medline Industries, LPSearch for the manufacturer's official notice
- News coverageRecent reporting on this recall and manufacturer
- openFDA data recordThe raw JSON record this page is built from
Source: U.S. FDA openFDA device enforcement reports. This summary is informational and may lag or differ from the official record. Always verify against the FDA before acting.
Taylor Coteus is RecallWatch's Legal News Analyst, covering FDA medical-device enforcement and patient-safety litigation. He reviews every recall against the FDA's official openFDA record before it is published and is responsible for corrections and editorial accuracy.
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