HIGHFDA DEVICE

Medline medical convenience kits labeled as: 1) TOTAL JOINT PACK Medline Kit SKU DYNJ65065A: 2) EXTREMITY/FOOT PACK Medline Kit SKU DYNJ65066B: 3) ANTERIOR CERVICAL-SMH Medline Kit SKU...

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.

Medline Industries, LPHealth & Personal CareMedical DevicesMedline Kit SKU DYNJ65065AUDI/DI 10193489317244 (each) 40193489317245 (case)Lot Number 24KMI926

Source-backed recall notice

No product image was available from the source feed.

Official source
FDA DEVICE
Recall date
June 11, 2026
Status
ACTIVE

Quick Facts at a Glance

Recall Date
June 11, 2026
Hazard Level
HIGH
Brand
Medline Industries, LP
Geographic Scope
9 states

What to Do Now

Use this page like a recall checklist: verify the product first, then act on the official remedy.

Immediate steps

  1. 1Stop using the product until you confirm whether it is included in the recall.
  2. 2Compare the product label, model number, UPC, color, size, and purchase location against the identifiers below.
  3. 3Follow the official remedy from FDA - Medical Devices; save photos, receipts, labels, and correspondence before contacting the company.
  4. 4If the product could harm a child, older adult, pet, or patient, move it out of reach immediately.

Check these identifiers

Brand
Medline Industries, LP
Model numbers
Medline Kit SKU DYNJ65065A, UDI/DI 10193489317244 (each) 40193489317245 (case), Lot Number 24KMI926, Lot Number 25BMI009, Lot Number 25DME458, Lot Number 25FMC143, Medline Kit SKU DYNJ65066B, UDI/DI 10193489317183 (each) 40193489317184 (case) +2 more
Where affected
CT, FL, KS, OH, NY, MD, MT, VA +1 more

Recall Timeline

Key dates and source checks for this recall record.

  1. Recall announced

    June 11, 2026

  2. Reported by FDA DEVICE

    July 29, 2026

  3. RecallRadar source check

    August 4, 2026

  4. Consumer action

    Use the official remedy and keep documentation.

Hazard Information

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.

What You Should Do

Patients and healthcare providers should stop using this device immediately. Follow the recall instructions provided by the manufacturer. Contact Medline Industries, LP or your healthcare provider for instructions. Notification method: Two or more of the following: Email, Fax, Letter, Press Release, Telephone, Visit

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Full Description

Medline medical convenience kits labeled as: 1) TOTAL JOINT PACK Medline Kit SKU DYNJ65065A: 2) EXTREMITY/FOOT PACK Medline Kit SKU DYNJ65066B: 3) ANTERIOR CERVICAL-SMH Medline Kit SKU DYNJ907718B: 4) LAMINECTOMY-SMH Medline Kit SKU DYNJ907732C: 5) KYPHOPLASTY Medline Kit SKU DYNJ907984C: 6) LUMBAR LAMINECTOMY Medline Kit SKU DYNJ907987D: 7) KYPHOPLASTY TRAY Medline Kit SKU DYNJ908413C: 8) CRANIOTOMY Medline Kit SKU DYNJ910626: 9) NEURO SPINE Medline Kit SKU DYNJ910639.. Reason: 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.. Classification: Class II. Quantity: 1601 units. Distribution: US: CT, FL, KS, OH, OR, NY, MD, MT, VA, MA.

Safety Guide

Not sure what to do next? Our guide walks you through the process step by step.

Read: How to Get Refunds and Replacements

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Product Classification

Product Details

Model Numbers
Medline Kit SKU DYNJ65065A
UDI/DI 10193489317244 (each) 40193489317245 (case)
Lot Number 24KMI926
Lot Number 25BMI009
Lot Number 25DME458
+5 more
Affected States
CT, FL, KS, OH, NY, MD, MT, VA, MA
Report Date
July 29, 2026
Recall Status
ACTIVE

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