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

Medline CCI Nerve Block Tray DYNJRA2742 Medline CPNB DYNJRA2716 recalled

Medline Industries is recalling Medline CCI Nerve Block Tray DYNJRA2742 Medline CPNB DYNJRA2716, 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 codesDYNJRA2742 UDI-DI 10198459627330 Lot 26AMA185 DYNJRA2716 UDI-DI 10198459567988 Lot 25KBA971
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-2415-2026
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 CCI Nerve Block Tray DYNJRA2742 Medline CPNB DYNJRA2716

Where it was distributed

US Nationwide distribution. OUS distribution pending.

Nationwide

Questions about this recall

Is Medline CCI Nerve Block Tray DYNJRA2742 Medline CPNB DYNJRA2716 recalled?

Yes. Medline Industries recalled Medline CCI Nerve Block Tray DYNJRA2742 Medline CPNB DYNJRA2716 on 27 Apr 2026. The recall is Class II and its status is Ongoing. Recall number Z-2415-2026.

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?

DYNJRA2742 UDI-DI 10198459627330 Lot 26AMA185 DYNJRA2716 UDI-DI 10198459567988 Lot 25KBA971

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

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