FDA Device Recalls

Recalls /

#211380

Product

Medline custom medical procedure kits labeled as: 1) MEM MAXILLOFACIAL PACK-LF, REF DYNJ0660040R; 2) FREE FLAP PACK-LF, REF DYNJ42833A; 3) FREE FLAP PACK-LF, REF DYNJ42833B; 4) TYMPANOPLASTY PACK, REF DYNJ50692C; 5) MAJOR CRANIOTOMY SAFETY, REF DYNJ54736B; 6) FREE FLAP CUSTOM PACK A, REF DYNJ82735; 7) NSR-SMR, REF DYNJ903144C; 8) KIT FACIAL MINORPLASTICS MOSES, REF DYNJ905365A; 9) SEPTOPLASTY, REF DYNJ906474; 10) SEPTOPLASTY, REF DYNJ906474A; 11) FREE FLAP, REF DYNJ907802; 12) MINOR DIEP, REF DYNJ907863; 13) MAIN FLAP, REF DYNJ908264.

FDA product code
FTNPlastic Surgery And Accessories Kit
Device class
Class 1
Medical specialty
General, Plastic Surgery
Affected lot / code info
1) REF DYNJ0660040R, UDI/DI 10889942220083 (EA) 40889942220084 (CS), Lot Numbers: 19BKB772, 19DKB804, 19FKB661, 19GKD118, 19IKA148, 19KKB086, 20AKB057, 20BKB114, 20FKB215, 20JKA546, 20LMA968, 20LMF795, 21DMA309, 21DMF310, 21FMA264, 21GMB043, 21HMD757, 21JMC608, 21KMH631, 22CMB438; 2) REF DYNJ42833A, UDI/DI 10888277503991 (EA) 40888277503992 (CS), Lot Numbers: 19ABS779, 19EBZ888, 19FBJ253, 19FBO513, 19FBX305, 19GBF427, 19LBY431, 20CBD972, 20DBV565, 20HBL275, 20LBA473, 20LBG895, 21CBI208; 3) REF DYNJ42833B, UDI/DI 10193489880335 (EA) 40193489880336 (CS), Lot Numbers: 21GBJ447, 21GBJ449, 21HBM834, 21HBR207, 22CBT921, 22DBM124, 22GBD852, 22HBF050, 22HBJ420, 22IBJ529, 22KBR876, 23BBA545, 23CBD715, 23CBQ582, 23DBH453, 23HBE012, 23HBR165, 23IBK906, 23KBP817, 24BBA648, 24DBD590, 24FBI859, 24GBU033, 24IBG868, 24JBI576; 4) REF DYNJ50692C, UDI/DI 10193489752199 (EA) 40193489752190 (CS), Lot Numbers: 19KDA566, 20BDC412, 20CDA575, 20GMD317, 21DMA002; 5) REF DYNJ54736B, UDI/DI 10889942925483 (EA) 40889942925484 (CS), Lot Numbers: 19ABB603, 19ABV222, 19CBN379, 19DBS122, 19EBZ894, 19FBQ049; 6) REF DYNJ82735, UDI/DI 10195327207540 (EA) 40195327207541 (CS), Lot Numbers: 22KMF252, 23EMG596, 23FMA429, 23IMA461, 23JMC236, 24BMC071; 7) REF DYNJ903144C, UDI/DI 10193489677881 (EA) 40193489677882 (CS), Lot Numbers: 19JBK003, 19SBD201, 20ABZ780, 20FBK295, 20GBR819, 20IBH005, 20LBK729, 20LBL461, 20LBO417, 20LBU129, 22AMA090, 22AMC790, 22BMF138, 22EMH876; 8) REF DYNJ905365A, UDI/DI 10193489759037 (EA) 40193489759038 (CS), Lot Numbers: 19IBR377, 20CBO773, 20GBI734, 20GBJ843, 20HBC012, 20IBQ906, 20JBO730, 21CBZ725, 21DBU031, 21GBF999, 21IBC232, 21VBB589; 9) REF DYNJ906474, UDI/DI 10193489750492 (EA) 40193489750493 (CS), Lot Numbers: 20ADB316, 20BDC489; 10) REF DYNJ906474A, UDI/DI 10193489344721 (EA) 40193489344722 (CS), Lot Numbers: 20EDC407, 20FDB425, 20HDA265, 20KDA931, 20KDC466, 21BDA054, 21EDA134, 21FDB465, 21GDB063, 21HDB526, 21IDA248; 11) REF DYNJ907802, UDI/DI 10193489890006 (EA) 40193489890007 (CS), Lot Numbers: 21GBI826, 22IBH914; 12) REF DYNJ907863, UDI/DI 10193489913187 (EA) 40193489913188 (CS), Lot Numbers: 21GBJ056, 21JBZ373, 21KBX700, 21LBV116; 13) REF DYNJ908264, UDI/DI 10195327020118 (EA) 40195327020119 (CS), Lot Numbers: 21LBU103.

Why it was recalled

Custom convenience kits are being recall because the contain non-sterile Codman Surgical Patties & Surgical Strips, which have the potential for endotoxin contamination.

Root cause (FDA determination)

Nonconforming Material/Component

Action the firm took

Medline issued a MEDICAL DEVICE VOLUNTARY RECALL notice on 11/21/2024 to its consignees via US Mail and email. The notice explained the issue, potential risk to health, and requested that the affected product be quarantined. Once the response is received, Medline will provide labels to place on affected inventory, with instructions for the consignee to remove the affected component prior to using the kit.

Recalling firm

Firm
MEDLINE INDUSTRIES, LP Northfield
Address
3 Lakes Dr, Northfield, Illinois 60093-2753

Distribution

Distribution pattern
Worldwide distribution - US Nationwide and the countries of UAE, and Canada.

Timeline

Recall initiated
2024-11-21
Posted by FDA
2024-12-30
Status

Source: openFDA Device Recall endpoint. Recall record ID #211380. The FDA issues recall classifications as health-hazard assessments, not legal findings; for legal claims consult a licensed attorney.