PlainRecalls
ModerateClass IIOngoing

FDA Devices recall · Reported June 24, 2026

Medline convenience kits: FEMORAL BLOCK TRAY DYNJRA1739B

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

Recall #
Z-2442-2026
Affected scope
49,654 kits total
Initiated
April 27, 2026
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Medline Industries, LP recalled Medline convenience kits: FEMORAL BLOCK TRAY DYNJRA1739B - a moderate-severity action.

Medline convenience kits: FEMORAL BLOCK TRAY DYNJRA1739B was recalled by Medline Industries, LP in June 24, 2026. Reason: Kits contain recalled lot of Ferndale Laboratories MASTISOL Liquid Adhesive. Butyrate tubing may crack during…. Check the official notice for the remedy. Verify recall #Z-2442-2026 with the FDA Devices before acting.

The recall

Medline Industries, LP issued this moderate-severity FDA Devices recall-Kits contain recalled lot of Ferndale Laboratories MASTISOL Liquid Adhesive. Butyrate tubing may crack during….

Moderate
severity level
Class II
classification
June 24, 2026
reported

Sourced from official FDA Devices enforcement records. Verify recall #Z-2442-2026 with the agency before acting. Full product description, hazard, remedy, and related recalls are below.

Recall Insight

This recall's affected scope, documented in the Recall Profile below, stays within a single-region or limited-distribution footprint. Distribution scope (see Distribution below) directly affects the consumer exposure window and determines whether a recall remains regional or escalates into a nationwide advisory.

Within the same product category the archive holds 6 closely related recalls, 6 from FDA Devices and 1 from Medline Industries, LP - clustering in a narrow category often points to a systemic quality-control or supplier issue rather than a one-off defect. Always verify the recall number against the official agency record before acting.

Medical Devices recalls over time

Where this recall sits in its category - 41,021 medical devices recalls on record

01,0002,0003,0004,000 20052008201120142017202020232026 1,947
Severity1906864652High severity (most serious)Moderate severityLow severity
Where this agency-classified recall sits among FDA Class I/II/III notices

Of 88,244 recalls with an agency hazard classification, 19,068 are high severity, 64,652 moderate, and 4,524 low. A further 16,179 CPSC/NHTSA recalls have no agency class and are excluded from this split. This recall is classified moderate severity.

Counts reflect market size and reporting activity, not inherent danger, we do not rank products by risk from raw recall volume.

Product description

Medline convenience kits: FEMORAL BLOCK TRAY DYNJRA1739B

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.

Recall Profile

Structured summary of the FDA Devices recall record
Attribute Value
Agency U.S. Food and Drug Administration
Severity class Moderate (Class II)
Status Ongoing
Recall number Z-2442-2026
Date reported June 24, 2026
Date initiated April 27, 2026
Recalling firm Medline Industries, LP
Firm location Northfield, IL
Affected scope 49,654 kits total
Distribution US Nationwide distribution. OUS distribution pending.

Profile values are sourced directly from the official FDA Devices enforcement record. Source: U.S. Food and Drug Administration.

What to do with this recall

Match your product against the recall record, then act on the agency remedy.

  • Check the recall number (Z-2442-2026) and product description against the item you own. Search the archive
  • Confirm the current status with FDA Devices before acting, recall details can be updated.
  • Follow the documented remedy (refund, replacement, repair, or disposal) rather than general advice. What to do next

This page summarizes the official FDA Devices record for research and awareness; it is not legal, medical, or safety advice. Verify with the issuing agency before acting.

Frequently Asked Questions

What product was recalled?
Medline convenience kits: FEMORAL BLOCK TRAY DYNJRA1739B. Recalled by Medline Industries, LP. Units affected: 49,654 kits total.
Why was this product recalled?
Kits contain recalled lot of Ferndale Laboratories MASTISOL Liquid Adhesive. Butyrate tubing may crack during actuation and render product unusable for application.
Which agency issued this recall?
This recall was issued by the FDA Devices on June 24, 2026. Severity: Moderate. Recall number: Z-2442-2026.
Where was the recalled product distributed?
Distribution: US Nationwide distribution. OUS distribution pending..
Should I stop using a recalled medication or medical device?
Do not stop using a recalled medication or device without consulting your healthcare provider first, as abruptly discontinuing treatment could pose its own health risks. Your doctor can advise on alternatives or whether the recall applies to your specific product lot. Check the recall number and lot information against your product packaging.

Nationwide recalls with similar severity or category timing

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This recall: FDA Devices, reported June 24, 2026. Severity classes follow each agency's own taxonomy; related-recall context is computed across the full archive.

Methodology · Corrections · Archive as of August 2026