Medline Convenience Kits Recall Issued
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Medline Industries is recalling 49,654 convenience kits nationwide because they contain a recalled lot of MASTISOL Liquid Adhesive with tubing that may crack.
What this FDA recall tells you, and what most readers miss
This notice was issued by FDA on August 3, 2026 and geographically references United States. Its severity classification of "medium" signals how the issuing agency weighs the risk of harm if no action is taken - "critical" and "high" tier alerts typically carry direct consumer actions, while "medium" and "low" tend toward informational guidance or monitoring advisories. The category it belongs to - FDA Recalls - determines the consumer-protection framework behind it, which shapes what remedies (refunds, replacements, repairs, or the recall itself) are available to affected consumers and which agency holds statutory responsibility for enforcement.
Most readers skim a notice like this, check whether they are personally affected, and move on. The more useful lens is to verify its scope, source, and timestamp, then compare related notices without assuming that one record proves a broader trend.
Areazine pairs this record with the original agency URL so you can check the primary source before acting. Its related labels are recall, product-safety, fda, medical-devices.
What Happened
Medline Industries, LP initiated a voluntary recall of certain convenience kits that contain a recalled lot of Ferndale Laboratories MASTISOL Liquid Adhesive. The butyrate tubing may crack during actuation and render the product unusable for application.
Which Products Are Affected
The recall covers 49,654 kits distributed nationwide in the United States. Affected products include:
- BIB AV FISTULA PACK DYNJ58304B (Lot 25LBP470)
- CARDIAC MINOR SURGICOUNT PACK DYNJ56573B (Lot 25KBK220)
- ENDOVASCULAR PACK DYNJ29135N (Lot 25LMG563)
- EP DEVICE DYNJ65916B (Lots 25KBG852, 25LBB895)
- FULL LINE ANEURYSM CDS CDS983672P (Lots 25LBO027, 26BBB852)
- GEN FEM POP #14-RF DYNJ21877W (Lot 25JBW040)
- IMPLANT PACK DYNJ39316D (Lot 25KBH774)
- OPEN HEART MRNGSD DYNJ58354F (Lot 25KBI240)
- PACEMAKER PACK-LF DYNJ0618174N (Lot 25KBC715)
- PACEMAKER SETUP PACK DYNJ35761D (Lot 26CBC772)
- PACER / CATH LAB PACK-LF DYNJ0972604A (Lot 25LMF965)
- PACER CDS CDS983686I (Lot 26ABE755)
- PACER PACK DYNJ52059D (Lots 25LBQ917, 26CBE736)
- PK, EP LAB PACEMAKER DYNJ43663A (Lot 26CBB662)
- VENOUS ACCESS PACK DYNJ45640B (Lot 25LMJ305)
This is FDA recall number Z-2444-2026, classified as Class II.
What You Should Do
Consumers in possession of the affected kits should follow instructions provided in the recall notification from Medline Industries, LP.
Why This Matters
The recall affects medical procedure kits used across the United States, potentially impacting availability of sterile supplies for various surgical and catheterization procedures.
Source
FDA Enforcement Report, recall Z-2444-2026 (https://www.fda.gov)
Original source: FDA Official Notice ↗
Related FDA Recalls
All FDA Recalls →Nationwide notices with similar length or severity timing 8
Two Areazine-derived peer sets for this FDA recall: nearest notices by body length and by same severity near the same agency date. Peers come from other categories so they are not the same-feed Related list above.
Similar body length
Nearest notices by article body length (1,640 characters here).
Similar severity timing
Same severity (medium) notices issued closest in time to August 3, 2026.
Frequently Asked Questions
Common questions about this FDA recall.