# FDA recall Z-2994-2026

> **Medline Industries, LP** · Class II · device recall initiated 2026-07-08.

## Product

Medline medical convenience kits, labeled as:    1) SINUS PACK-LF, Medline Kit SKU DYNJ0966146F;   2) ENT PACK, Medline Kit SKU DYNJ40154D;   3) ENT PACK, Medline Kit SKU DYNJ40154F;   4) ENT SCOPE PACK, Medline Kit SKU DYNJ44480D;   5) ENT NASAL ORAL PACK MOSES, Medline Kit SKU DYNJ58928A;   6) HEAD & NECK PACK, Medline Kit SKU DYNJ83296;   7) TRANSPHENOIDAL PACK, Medline Kit SKU DYNJ89006;   8) SINUS, Medline Kit SKU DYNJ900537D;   9) SINUS, Medline Kit SKU DYNJ900537F;   10) ENT HEAD & NECK, Medline Kit SKU DYNJ903679F;   11) ENT HEAD & NECK, Medline Kit SKU DYNJ903679G;   12) ENT HEAD & NECK, Medline Kit SKU DYNJ903679I;   13) ENT HEAD & NECK, Medline Kit SKU DYNJ903679J;   14) ENT HEAD & NECK, Medline Kit SKU DYNJ903679K.

## Reason for recall

Specific item(s) and lot(s) of Medline convenience kits containing Pilling Wecksorb Neurosponges and Neurosponge Strips are being recalled due to potential out-of-specification levels of endotoxin of the neurosponges.

## Distribution

US Nationwide distribution in the states of AZ, CA, IA, ID, IL, IN, MA, MD, MI, MN, MO, MT, NY, OH, TX, WI, WY.

## Key facts

- **Recall number:** Z-2994-2026
- **Recalling firm:** Medline Industries, LP
- **Classification:** Class II
- **Product type:** device
- **Status:** Ongoing
- **Initiation date:** 2026-07-08
- **Report date:** 2026-09-02

- **Voluntary/Mandated:** Voluntary: Firm initiated
- **Location:** Northfield, IL, United States

## Primary source

FDA Enforcement Reports: https://www.accessdata.fda.gov/scripts/ires/index.cfm?Product=Z-2994-2026

## Citation

> MORVS. FDA recall Z-2994-2026. Retrieved 2026-10-20 from https://api.morvs.ai/recall/Z-2994-2026. Source: US FDA. Licensed CC0.

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*[Dataset catalog](/datasets/) · [FDA recalls dataset](/datasets/fda-recalls) · CC0 1.0*