Medline Industries recall: Medline convenience kits containing Healthmark Instrument Channel Brushes
Medline Industries, LP is recalling Medline convenience kits containing Healthmark Instrument Channel Brushes – 90 kits (US). The U.S. Food and Drug Administration published the recall on September 30, 2026; it began on August 10, 2026. Distributed nationwide.
Serious Class II means the product may cause temporary or medically reversible health problems, or the chance of serious harm is remote.
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| Product | Medline convenience kits containing Healthmark Instrument Channel Brushes |
| Brand | Medline Industries |
| Company | Medline Industries, LP |
| Type | Medical devices |
| Classification | Class II |
| Recall date | August 10, 2026 |
| Published by FDA | September 30, 2026 |
| Quantity | 90 kits (US) |
| Recall ID | 99729 |
Recalled products (2)
- Medline convenience kits containing Healthmark Instrument Channel Brushes. SINUS PACK DYNJ48258D and Sinus Pack DYNJ48258F.
- FDA recall number
- Z-3229-2026
- Codes, lots and dates
- DYNJ48258D UDI-DI 10889942563272 Lots 23CBH459 23GBJ128 24ABM400
- Quantity
- 90 kits (US)
- Classification
- Class II
- Medline convenience kits containing Healthmark Instrument Channel Brushes. SINUS PACK DYNJ48258D and SINUS PACK DYNJ48258F.
- FDA recall number
- Z-3230-2026
- Codes, lots and dates
- DYNJ48258F UDI-DI 10198459038334 Lots 24HBR684 25CBS234 25GBH438 25JBC863 26FBU052
- Quantity
- 90 kits (US)
- Classification
- Class II
Identifiers and details
- FDA event ID
- 99729
- Initiated
- Voluntary: Firm initiated
- Status
- Ongoing
- Firm location
- Northfield, IL, United States
Why it was recalled
The reason the FDA lists: “Kits contain Healthmark Instrument Channel Brushes, which were recalled by the manufacturer due to the potential for a sharp edge/burr on the end of the brush. Potential hazards associated include cut injury/abrasion and infection.”
Where it was sold
Nationwide. Distribution as the FDA records it: “US Nationwide distribution in the states of MN and SD.”
What to do
Compare the recall numbers, lot numbers and expiration dates with what you have. Do not stop a prescribed medicine or device without talking to your pharmacist or doctor – they can arrange a replacement from an unaffected lot.
Official notice: FDA Enforcement Report record (event 99729, openFDA) – the same recall numbers can be searched in the FDA Enforcement Report.
Other Medline Industries recalls
| Date | Recall | Problem | Agency |
|---|---|---|---|
| Oct 7, 2026 |  Medline Industries recall: Medline Basic Homecare Beds and Medlite Homecare Beds and Accessories and 1 more productMedical devices · 771,127 total | a fire hazard Most serious | FDA Class I |
| Sep 30, 2026 | Medline Industries recall: Medline Convenience Kits: 1) PEDS SINUS PACK and 4 more productsMedical devices · 695 kits; 128 kits; 486 kits; 234 kits; 4013 kits | The kits contain neurological sponges with the potential for unexpected variability of end… Serious | FDA Class II |
| Sep 23, 2026 | Medline Industries recall: Medline Convenience Kits: 1) KIT ANESTHESIA L&D A- LINE SET and 6 more productsMedical devices · 12 kits; 489 kits; 447 kits; 10407 kits; 2718 kits; 1100 kits; 47848 kits | The kits contain certain lots of sterile applicators which may contain fungal contaminatio… Most serious | FDA Class I |
| Sep 23, 2026 | Medline Industries recall: Convenience kits ANESTHESIA PAIN PK LEAGUE DYNJ67925A and 3 more productsMedical devices · 341; 459; 60; 336 | a sterility problem Serious | FDA Class II |
| Sep 23, 2026 | Medline Industries recall: Medline Convenience Kit: OPEN HEART A PACKMedical devices · 135 units | a sterility problem Serious | FDA Class II |
| Sep 9, 2026 | Medline Industries recall: Medline Convenience Kits containing BD ChloraPrep ClearMedical devices · 222,653 total | Convenience kits contain BD ChloraPrep Clear - 1mL Applicators from specific lots that wer… Serious | FDA Class II |
| Sep 9, 2026 | Medline Industries recall: Medline Convenience Kits: 1) DRAWER 9 CRICOTHYROTOMY KIT and 15 more productsMedical devices · 104 kits; 4636 kits; 58037 kits; 17,750 kits; 176 kits; 300 kits; 434,595 kits; 1840 kits; 22736 Kits; 3650 kits; 13032 kits; 3752 kits; 352 kits; 2080 kits; 18290 kits; 996692 kits | a sterility problem Serious | FDA Class II |
| Sep 2, 2026 | Medline Industries recall: Medline medical convenience kit labeled as: TRACH TUBE KITMedical devices · 45 kits | Component labeling discrepancy Serious | FDA Class II |
| Sep 2, 2026 | Medline Industries recall: Medline medical convenience kitsMedical devices · 2262 kits; 246 kits; 3468 kits; 974 kits | Specific item(s) and lot(s) of Medline convenience kits containing Pilling Wecksorb Neuros… Serious | FDA Class II |
| Sep 2, 2026 | Medline Industries recall: Medline Hudson RCI and 2 more productsMedical devices · 20 units; 145525 units; 271406 units | Neonatal and infant heated wire breathing circuits may experience sporadic failure. The he… Serious | FDA Class II |
| Sep 2, 2026 | Medline Industries recall: Medline convenience kits labeled as: 1) FEMORAL PACK and 10 more productsMedical devices · 71 kits; 263 kits; 24 kits; 94 kits; 15 kits; 663 kits; 1349 kits; 106 kits; 169 kits; 419 kits; 241 kits | Kits contain a potentially contaminated component which were recalled by the manufacturer Serious | FDA Class II |
| Aug 19, 2026 | Medline Industries recall: Medline Micro-Kill Bleach Germicidal Bleach WipesMedical devices · 591,561 units; 447,618 units; 1,244 units; 31,728 | Medline Micro-Kill Bleach Germicidal Bleach Wipes may exhibit a reduction in bleach concen… Serious | FDA Class II |
All 13 Medline Industries recalls →
About this recall
Is Medline Industries Medline convenience kits containing Healthmark Instrument Channel Brushes recalled?
Yes. Medline Industries, LP recalled it on August 10, 2026; FDA published it September 30, 2026 (Class II). Only the lots, dates or models listed on this page are included.
Why was it recalled?
Kits contain Healthmark Instrument Channel Brushes, which were recalled by the manufacturer due to the potential for a sharp edge/burr on the end of the brush. Potential hazards associated include cut injury/abrasion and infection.
What should I do if I have it?
Compare the recall numbers, lot numbers and expiration dates with what you have. Do not stop a prescribed medicine or device without talking to your pharmacist or doctor – they can arrange a replacement from an unaffected lot.
Where was it sold?
Nationwide.
More recalls
Source: recall records published by the U.S. Food and Drug Administration (openFDA Enforcement Reports), the USDA Food Safety and Inspection Service, the Consumer Product Safety Commission and the National Highway Traffic Safety Administration, collected twice a day. Product names, lot codes, dates and model numbers are shown exactly as the agency lists them; the agency's notice is the authority. 77.today is not affiliated with any of these agencies.