---
title: "MEDLINE Polyurethane Foam Enzymatic Cleaning Sponge, REF DYK1000TSE — FDA record Z-1217-2022 | Is It on Recall"
description: "Sporadic reports were received of discoloration on the foam sponge on certain lots of the product, which has been identified as microbial contamination."
url: https://isitonrecall.com/recall/fda-device-z-1217-2022-medline-polyurethane-foam-enzymatic-cleaning-sponge-ref-dyk1000tse/
updated: 2026-10-01
site: "Is It on Recall"
language: en
---

[Recall archive](https://isitonrecall.com/archives/) / FDA device enforcement

# MEDLINE Polyurethane Foam Enzymatic Cleaning Sponge, REF DYK1000TSE — FDA record Z-1217-2022

Reported ongoing

Status as reported in the agency record. FDA warns that enforcement status may not track the current recall lifecycle; check the current official notice.

Source date Apr 21, 2022. Retrieved Oct 1, 2026. Last updated Oct 1, 2026.

Archive changed Oct 1, 2026. USDA FSIS records are unavailable; [check FSIS directly](https://www.fsis.usda.gov/recalls). [Source coverage and dates](https://isitonrecall.com/sources/).

## What the record says

- **Product**: MEDLINE Polyurethane Foam Enzymatic Cleaning Sponge, REF DYK1000TSE
- **Reason**: Sporadic reports were received of discoloration on the foam sponge on certain lots of the product, which has been identified as microbial contamination.
- **Classification**: Class II
- **Recalling firm**: MEDLINE INDUSTRIES, LP - Northfield
- **Quantity**: 500 boxes of 100 units
- **Agency-reported status**: Ongoing
- **Source record identifier**: Z-1217-2022

[Open the official record](https://api.fda.gov/device/enforcement.json?search=recall_number%3A%22Z-1217-2022%22)

[What the recall classes mean](https://isitonrecall.com/guides/recall-classes/). Classification is an agency assessment, not individual medical advice.

## Lot and product identifiers

| Label field | Details supplied by the agency |
| --- | --- |
| Lot, code or applicability | DI: (01) 40888277367358; All Envirolite lot numbers which have the following format on individual packaging: YYMMDD X where YY is last 2 digits of Year of production, MM is the number of the month of production, DD is the day of production and X is the leading number of the raw material batch number. |

Match all identifying details in the current notice. A brand name alone is not enough.

## Distribution

US and Panama

No US distribution state could be established from this record. Check the official notice.

## Dates in the source

- **Report date**: Jun 8, 2022
- **Recall initiation date**: Apr 21, 2022
- **Center classification date**: Jun 2, 2022

FDA company pages use the listing date; enforcement records use initiation dates; CPSC uses recall date; NHTSA uses report-received date. These dates are not interchangeable.

## What to do next

Read the official notice for the action that applies to your exact product.

[Read the current instructions](https://api.fda.gov/device/enforcement.json?search=recall_number%3A%22Z-1217-2022%22)

## Related records

[Medical devices records](https://isitonrecall.com/category/medical-devices/) [MEDLINE INDUSTRIES, LP - Northfield records](https://isitonrecall.com/brand/medline-industries-lp-northfield/)