FDA Device recall Z-1217-2022
MEDLINE Polyurethane Foam Enzymatic Cleaning Sponge, REF DYK1000TSE
- FDA Device
- Class II
- ongoing
- Published 2022-06-08
On 2022-06-08 the FDA classified a Class II recall of MEDLINE Polyurethane Foam Enzymatic Cleaning Sponge, REF DYK1000TSE by Medline Industries Northfield, citing sporadic reports were received of discoloration on the foam sponge on certain lots of the product, which has been identified as microbial contamination.
Read the official FDA Device notice
| Agency | FDA Device |
|---|---|
| Recall number | Z-1217-2022 |
| Classification | Class II |
| Status | ongoing |
| Initiated | 2022-04-21 |
| Published | 2022-06-08 |
| Last updated | 2026-09-13 11:56 UTC |
| Company | Medline Industries Northfield |
| Distribution | n/a |
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.
Identifiers
| code_info | DI: (01) 40888277367358; All Envirolite lot numbers which have the following format on individual packaging: YYMMDD X…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. |
|---|
Status history
No status changes recorded since RecallRadar first saw this recall on 2026-09-13 11:56 UTC. Current status: ongoing.
Source
Official record: https://api.fda.gov/device/enforcement.json?search=recall_number:%22Z-1217-2022%22
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