FDA Device recall Z-0696-2022

MEDLINE Micro-Kill Bleach Germicidal Bleach Wipes

FDA Device
Class II
ongoing
Published 2022-03-09

On 2022-03-09 the FDA classified a Class II recall of MEDLINE Micro-Kill Bleach Germicidal Bleach Wipes by Medline Industries Northfield, citing micro-Kill Bleach Wipes contain out of specification (low) levels of Sodium Hypochlorite.

Read the official FDA Device notice

Agency	FDA Device
Recall number	Z-0696-2022
Classification	Class II
Status	ongoing
Initiated	2021-12-29
Published	2022-03-09
Last updated	2026-09-13 11:56 UTC
Company	Medline Industries Northfield
Distribution	US

Product

MEDLINE Micro-Kill Bleach Germicidal Bleach Wipes

Reason

Micro-Kill Bleach Wipes contain out of specification (low) levels of Sodium Hypochlorite.

Identifiers

code_info	a. Model No.: MSC351400AN; UDI: 10888277652514; Lot No.: 209 and Batch ID: 20083 Lot No.: 210 and Batch ID: 20085 Lo… a. Model No.: MSC351400AN; UDI: 10888277652514; Lot No.: 209 and Batch ID: 20083 Lot No.: 210 and Batch ID: 20085 Lot No.: 211 and Batch ID: 20083 and 20084 Lot No.: 212 and Batch ID: 20084 and 20085 Lot No.: 213 and Batch ID: 20085 and 20086 Lot No.: 214 and Batch ID: 20086 and 20087 Lot No.: 215 and Batch ID: 20087 Lot No.: 216 and Batch ID: 20087 and 20090 Lot No.: 217 and Batch ID: 20090 Lot No.: 218 and Batch ID: 20090 and 20091 Lot No.: 231 and Batch ID: 20104 and 20105 Lot No.: 233 and Batch ID: 20105, 20106, and 20107 Lot No.: 235 and Batch ID: 20107 and 20108 Lot No.: 236 and Batch ID: 20108, 20109, and 20111 Lot No.: 238 and Batch ID: 20111 and 20112 Lot No.: 240 and Batch ID: 20112 and 20113 Lot No.: 241 and Batch ID: 20113 and 20114 Lot No.: 243 and Batch ID: 20114 and 20115 Lot No.: 244 and Batch ID: 20115 Lot No.: 245 and Batch ID: 20115 and 20118 Lot No.: 246 and Batch ID: 20118 Lot No.: 247 and Batch ID: 20118 and 20119 Lot No.: 248 and Batch ID: 20119 Lot No.:

code_info

a. Model No.: MSC351400AN; UDI: 10888277652514; Lot No.: 209 and Batch ID: 20083 Lot No.: 210 and Batch ID: 20085 Lo…

a. Model No.: MSC351400AN; UDI: 10888277652514; Lot No.: 209 and Batch ID: 20083 Lot No.: 210 and Batch ID: 20085 Lot No.: 211 and Batch ID: 20083 and 20084 Lot No.: 212 and Batch ID: 20084 and 20085 Lot No.: 213 and Batch ID: 20085 and 20086 Lot No.: 214 and Batch ID: 20086 and 20087 Lot No.: 215 and Batch ID: 20087 Lot No.: 216 and Batch ID: 20087 and 20090 Lot No.: 217 and Batch ID: 20090 Lot No.: 218 and Batch ID: 20090 and 20091 Lot No.: 231 and Batch ID: 20104 and 20105 Lot No.: 233 and Batch ID: 20105, 20106, and 20107 Lot No.: 235 and Batch ID: 20107 and 20108 Lot No.: 236 and Batch ID: 20108, 20109, and 20111 Lot No.: 238 and Batch ID: 20111 and 20112 Lot No.: 240 and Batch ID: 20112 and 20113 Lot No.: 241 and Batch ID: 20113 and 20114 Lot No.: 243 and Batch ID: 20114 and 20115 Lot No.: 244 and Batch ID: 20115 Lot No.: 245 and Batch ID: 20115 and 20118 Lot No.: 246 and Batch ID: 20118 Lot No.: 247 and Batch ID: 20118 and 20119 Lot No.: 248 and Batch ID: 20119 Lot No.:

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-0696-2022%22

RecallRadar indexes public recall notices from the FDA, USDA FSIS, and CPSC. The official agency notice is the authoritative source. Always confirm details at the linked source before acting.