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RecallWatchMedical Device Safety
Class IIOngoingZ-2431-2026

Medline Industries, LP recalls Medline convenience kits: DAVINCI DYNJ905836D DAVINCI-LF DYNJ905293I GENERAL…

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: DAVINCI DYNJ905836D DAVINCI-LF DYNJ905293I GENERAL ROBOTICS PACK DYNJT8308 GYN LAP CDS860087Q GYN LAPAROSCOPY DYNJ910084C GYN LAPAROSCOPY CDS CDS982371I GYN LAPAROSCOPY CDS #34-RF CDS920099S GYN LAPAROSCOPY PACK DYNJT3887 DYNJT6876 GYN ROBOTIC CDS CDS984228K GYN ROBOTICS DYNJ911843 KIT LABOR DELIVERY TUBAL LIGAT DYKMBNDL165C ROBOTIC LAP CHOLE CDS CDS985442J ROBOTIC PACK DYNJ84725B DYNJ910594B ROBOTIC SURGERY PACK DYNJ53711B ROBOTICS PACK DYNJ83622C UOFL GYN LAPAROSCOPY DYNJ909322B WMC ROBOTIC PACK - LFDYNJ902583O
    UDI-DI 10195327517977
    59 affected lots
    25LBB534DYNJ905293I1019845924797225KBM585DYNJT83081019845969713526CBD040CDS860087Q
    +51 more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

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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