CLASS II ONGOING Device recall · Reported 24 Jun 2026 · FDA Enforcement Report

Medline convenience kits: Femoral Block Tray DYNJRA1739B recalled

Medline Industries is recalling Medline convenience kits: Femoral Block Tray DYNJRA1739B, distributed nationwide in the US. The recall was initiated on 27 Apr 2026 and the FDA has classified it as Class II.

Check your package

Lot, batch or date codesDYNJRA1739B UDI-DI 10195327411237 Lot 25LBB731
Quantity recalled49,654 kits total

Stop using the device if the notice says to, and contact the manufacturer or your healthcare provider for the correction or replacement.

Recall details

Recall number
Z-2442-2026
FDA event ID
98951
Recalling firm
Medline Industries, Northfield, IL
Classification
Class II
Status
Ongoing
Recall initiated
27 Apr 2026
FDA classified
12 Jun 2026
Reported
24 Jun 2026
Type
Voluntary: Firm initiated
Customers notified by
Two or more of the following: Email, Fax, Letter, Press Release, Telephone, Visit
Reason category
Device Malfunction

Timeline

27 Apr 2026Recall initiated by company
12 Jun 2026Classified by FDA+46 days
24 Jun 2026Published in enforcement report+12 days

Companies usually start a recall weeks before the FDA classifies and publishes it; the gap above is that lag.

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.

Device recalls are issued when a component, software or design fault could cause the device to fail or give wrong readings. Many are corrections applied in the field rather than physical returns.

Product as listed by the FDA

Medline convenience kits: FEMORAL BLOCK TRAY DYNJRA1739B

Where it was distributed

US Nationwide distribution. OUS distribution pending.

Nationwide

Questions about this recall

Why was it recalled?

Kits contain recalled lot of Ferndale Laboratories MASTISOL Liquid Adhesive. Butyrate tubing may crack during actuation and render product unusable for application.

Which lots are affected?

DYNJRA1739B UDI-DI 10195327411237 Lot 25LBB731

Where was it sold?

US Nationwide distribution. OUS distribution pending.

What should I do if I have it?

Stop using the device if the notice says to, and contact the manufacturer or your healthcare provider for the correction or replacement.

What does Class II mean?

Class II means the product may cause temporary or medically reversible health problems, or the probability of serious harm is remote.

Read the official FDA notice · Source record retrieved 26 Sep 2026. The FDA describes openFDA data as unvalidated; the official notice takes precedence. This page reports the record and gives no medical advice.

Other products in this recall event

33 other products · FDA event 98951

This product is part of a recall event; the main page for the event is Medline convenience kits: Cmh Central Line Dressing Change recalled.

ReportedClassRecallCompanyReasonWhere
CLASS IIMedline convenience kits: Cmh Central Line Dressing Change recalledMedline IndustriesDevice MalfunctionNationwide
CLASS IIMedline convenience kits: Davinci Main DYNJ908031D recalledMedline IndustriesDevice MalfunctionNationwide
CLASS IIMedline convenience kits: Acd DYNJ904999J Acdf DYNJ907336B recalledMedline IndustriesDevice MalfunctionNationwide
CLASS IIMedline convenience kits: Davinci DYNJ905836D Davinci-lf recalledMedline IndustriesDevice MalfunctionNationwide
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CLASS IIMedline convenience kit: IV Start Kit W/Hubguard DYNDV2662 recalledMedline IndustriesDevice MalfunctionNationwide
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CLASS IIMedline convenience kit: Bhs Neuro DYNJ904900N Medtrx Neuro recalledMedline IndustriesDevice MalfunctionNationwide
CLASS IIMedline convenience kits: Acl Pack DYNJ64161C Arthroscopy recalledMedline IndustriesDevice MalfunctionNationwide
CLASS IIMedline convenience kits: Discectomy Pack DYNJ86476B Ear recalledMedline IndustriesDevice MalfunctionNationwide
CLASS IIMedline convenience kit: Kit: Dressing Change Ped DYNDC3359 recalledMedline IndustriesDevice MalfunctionNationwide
CLASS IIMedline convenience kits: Basic Eye DYNJ905154I Tubal recalledMedline IndustriesDevice MalfunctionNationwide
CLASS IIMedline convenience kits: CVC Insertion KIT ECVC6805B recalledMedline IndustriesDevice MalfunctionNationwide
CLASS IIMedline convenience kits: Loop Pack DYNJ61460C Open Heart recalledMedline IndustriesDevice MalfunctionNationwide
CLASS IIMedline convenience kits: Port A Cath DYNJ906818A recalledMedline IndustriesDevice MalfunctionNationwide

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