Medline Convenience Kits Recall Issued
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Medline Industries is recalling 1,601 units of specific medical convenience kits containing BD PurPrep 26 mL potentially contaminated with Bacillus species.
What this FDA recall tells you, and what most readers miss
This notice was issued by FDA on August 12, 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 is issuing a recall for specific Medline convenience kits containing BD PurPrep 26 mL which may be contaminated with low levels of Bacillus species.
Which Products Are Affected
The recall covers 1601 units distributed in CT, FL, KS, OH, OR, NY, MD, MT, VA, and MA. Affected products include:
- TOTAL JOINT PACK (Medline Kit SKU DYNJ65065A) with multiple lots including 24KMI926, 25BMI009, 25DME458, 25FMC143
- EXTREMITY/FOOT PACK (Medline Kit SKU DYNJ65066B) with multiple lots including 24KME109, 24LMD416, 25BMB162, 25DMB403, 25DMK347, 25FMA695
- ANTERIOR CERVICAL-SMH (Medline Kit SKU DYNJ907718B) with lots 25ABJ808, 25ABM644, 25BBT262
- LAMINECTOMY-SMH (Medline Kit SKU DYNJ907732C) with lots 24LBD661, 25ABP134, 25BBS412, 25DBS673, 25FBS372
- KYPHOPLASTY (Medline Kit SKU DYNJ907984C) with lot 25CBO351
- LUMBAR LAMINECTOMY (Medline Kit SKU DYNJ907987D) with multiple lots including 24LBO744, 25ABD265, 25CBD596, 25CBO352, 25EBB260, 25EBV317
- KYPHOPLASTY TRAY (Medline Kit SKU DYNJ908413C) with lots 25EBD582, 25FBM835
- CRANIOTOMY (Medline Kit SKU DYNJ910626) with lots 25DBC117, 25DBE196, 25FBL400
- NEURO SPINE (Medline Kit SKU DYNJ910639) with lots 24LBD222, 24LBN441, 25ABL748, 25EBF179, 25FBF363 Full UDI/DI and lot details are listed in the recall.
What You Should Do
Consumers should stop using the affected kits and contact Medline Industries, LP for return or refund instructions.
Why This Matters
The recall addresses potential contamination in surgical convenience kits distributed across multiple U.S. states.
Source
FDA recall number Z-2791-2026, event ID 99329.
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 (1,639 characters here).
Similar severity timing
Same severity (medium) notices issued closest in time to August 12, 2026.
Frequently Asked Questions
Common questions about this FDA recall.