MEDLINE Micro-Kill Bleach Germicidal Bleach Wipes
Medical device recall Z-0696-2022. Published in FDA’s Enforcement Report on Mar 9, 2022.
No Watch here, and no alerts: openFDA asks that its enforcement data “should not be used as a method to collect data to issue alerts to the public, nor should it be used to track the lifecycle of a recall” (openFDA). For FDA’s own recall emails, subscribe at FDA. FDA’s own record is on accessdata.fda.gov.
The short answer
Published in FDA’s Enforcement Report on Mar 9, 2022. Copied from openFDA on Oct 20, 2026.
- Class II FDA’s class
- Ongoing its status, in FDA’s file
- Nationwide FDA’s word for where it went
- 359,524 units how much, in FDA’s words
Every line below is in FDA’s own words, with its source beside it. FDA’s terms are explained in FDA’s own words.
How serious is it, by FDA’s class?
Class II, the middle of FDA’s three classes.
“Products that might cause a temporary health problem, or pose only a slight threat of a serious nature. Example: a drug that is under-strength but that is not used to treat life-threatening situations.”
openFDA, in plain words, its enforcement report fields.
“Class II is a situation in which use of, or exposure to, a violative product may cause temporary or medically reversible adverse health consequences or where the probability of serious adverse health consequences is remote.”
FDA’s rule, 21 CFR 7.3(m)(2), eCFR.
What these words mean is quoted from openFDA’s field reference and 21 CFR 7.3.
What’s wrong with it?
Micro-Kill Bleach Wipes contain out of specification (low) levels of Sodium Hypochlorite.
FDA, Device recall enforcement reports. Released Oct 14, 2026. Updated weekly.
Which ones are recalled?
MEDLINE Micro-Kill Bleach Germicidal Bleach Wipes
359,524 units, in FDA’s words.
FDA, Device recall enforcement reports. Released Oct 14, 2026. Updated weekly.
Codes to check against yours
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…
Every code shown here, 1,997 characters
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.: 249 and Batch ID: 20119 and 20120 Lot No.: 250 and Batch ID: 20120 Lot No.: 254 and Batch ID: 20132 Lot No.: 256 and Batch ID: 20132and 20133 Lot No.: 258 and Batch ID: 20136 and 20137 Lot No.: 260 and Batch ID: 20137 and 20139 Lot No.: 261 and Batch ID: 20139 and 20140 Lot No.: 263 and Batch ID: 20140 and 20141 Lot No.: 264 and Batch ID: 20141 and 20142 Lot No.: 288 and Batch ID: 20219 Lot No.: 289 and Batch ID: 20219 and 20220 Lot No.: 290 and Batch ID: 20220 and 20221 Lot No.: 291 and Batch ID: 20221 and 20223 Lot No.: 292 and Batch ID: 20223 and 20224 Lot No.: 293 and Batch ID: 20224, 20225, and 20232 Lot No.: 301 and Batch ID: 20293 and 20294 Lot No.: 302 and Batch ID: 20294 and 20295 Lot No.: 303 and Batch ID: 20295 and 20296 Lot No.: 304 and Batch ID: 20296 Lot No.: 305 and Batch ID: 20297, 20300, and 20301 Lot No.: 306 and Batch ID: 20300, 20301, and 20424 Lot No.: 307 and Batch ID: 20315 Lot No.: 308 and Batch ID: 20315 and 20316 Lot No.: 309 and Batch ID: 20316 and 20317 Lot No.:…
FDA’s list runs to 5,555 characters. The first part is shown; the rest is on FDA’s record.
Copied exactly as FDA lists them: lot and serial numbers, dates and other codes on the product or its label.
Where did it go?
FDA’s words for the “general area of initial distribution”: where the firm first shipped it.
Worldwide distribution - US Nationwide and the countries of Panama and Bermuda.
These words name no state.
What FDA means by nationwide
“The term “nationwide” is defined to mean the fifty states or a significant portion. Note that subsequent distribution by the consignees to other parties may not be included.”
openFDA, its enforcement report fields.
The words say it went outside the United States too.
What these words mean is quoted from openFDA’s field reference and 21 CFR 7.3.
Is it still going on?
Ongoing, in FDA’s file.
“A recall which is currently in progress.”
openFDA, on “On-Going”, its enforcement report fields.
What these words mean is quoted from openFDA’s field reference and 21 CFR 7.3.
- The firm began the recall on Dec 29, 2021.
- FDA classified it on Mar 1, 2022.
- FDA’s Enforcement Report published it on Mar 9, 2022.
FDA, Device recall enforcement reports. Released Oct 14, 2026. Updated weekly.
Who is recalling it?
- MEDLINE INDUSTRIES, LP - Northfield, of Northfield, IL.
- Who began it, in FDA’s words: Voluntary: Firm initiated.
- How the firm first told its customers: Letter.
FDA, Device recall enforcement reports. Released Oct 14, 2026. Updated weekly.
What this record can’t tell you
- Whether your own one is affected: compare the codes, dates and numbers above with yours. When unsure, ask the firm or the store.
- Where it went after the firm’s first shipments. FDA’s words cover the firm’s initial distribution, and, in FDA’s words, “subsequent distribution by the consignees to other parties may not be included.”
- How many have been returned, corrected or destroyed: FDA’s report doesn’t say.
- Whether anyone was hurt or fell ill: the report doesn’t say.
- How current it is: openFDA publishes FDA’s Enforcement Report weekly, after FDA does, and a firm can announce a recall weeks before it appears there. openFDA’s own caution: “This data should not be used as a method to collect data to issue alerts to the public, nor should it be used to track the lifecycle of a recall.”
- FDA’s list of codes runs to 5,555 characters; the first part is shown here, and the rest is on FDA’s record.
- A product with no recall here isn’t safe by that: FDA’s report lists the recalls FDA classified, and when.
Hearth Record wrote these lines; the quotations are FDA’s.
Sources
-
U.S. Food and Drug Administration, Device recall enforcement reports.
Released Oct 14, 2026 and checked Oct 20, 2026. Updated weekly. Public domain (CC0 1.0, openFDA). FDA asks that nothing suggest it endorses this site.
Recalls of food, medicines, medical devices, pet food and animal drugs are from the U.S. Food and Drug Administration (FDA). FDA does not endorse Hearth Record. openFDA: “Do not rely on openFDA to make decisions regarding medical care.” Copied on Oct 20, 2026.