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RecallWatchMedical Device Safety
Class IIOngoingZ-2423-2026

Medline Industries, LP recalls Medline convenience kits: BREAST IMAGING DYNJT5893 CHOG PLASTICS SYNJ10306A…

Medline Industries, LPNorthfield, IL, United StatesReported Jun 24, 2026 · 24 days ago
Legal News Analyst ·

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: BREAST IMAGING DYNJT5893 CHOG PLASTICS SYNJ10306A ENDO BREAST AUGMENTATION PACK DYNJ68023 FACIAL PLASTIC DYNJ909926C JVL - MODULE PLASTIC PK DYNJ84081B KIT MAJOR PLASTICS MOSES DYNJ905362C MEM MAXILLOFACIAL PACK-LF DYNJ0660040R MINOR BREAST PACK DYNJ89023A PLASTIC MAJOR SURGERY DYNJ902510M PLASTIC PACK DYNJ84766 PLASTIC PACK-LF DYNJ0578842M PLASTICS EXTREMITY PACK DYNJ63803C PLASTICS PK - NO SYR DYNJ62433D RR-ASC-RHINOPLASTY PACK-LF DYNJ81772C TRANSGENDER PACK DYNJT7588 WH PLASTIC MAJOR PACKDYNJ89048A
    UDI-DI 10198459517839
    54 affected lots
    25KBA123SYNJ10306A1019348929689125LBO30526CBD081DYNJ680231019348946808325KBI169
    +46 moreDYNJ909926C1019845942310925LBC06725LBR659DYNJ84081B1019845946247425LMI881DYNJ905362C1019845934684225KBN23925LBF694DYNJ0660040R1088994222008325JME57226AMA936DYNJ89023A1019845938831625KBC500DYNJ902510M1019845968337426CBM27926CBO942DYNJ847661019532741410826BBC049DYNJ0578842M1019348928829225LMG027DYNJ63803C1019845914982525LBN47626CBC156DYNJ62433D1019845949817625KBC75225KBM917DYNJ81772C1019845934936225LMH59425LMI396DYNJT75881019845963518226AMA250DYNJ89048A1019845938847726BBD124

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 details

US Nationwide distribution. OUS distribution pending.

Class IIWhat this means

Use of the product may cause temporary or medically reversible adverse health consequences.

Sources & references

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
Legal News Analyst

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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