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Class II: temporary or reversible health riskTerminated

Medline Industries Hand Sanitizer Foam Recall

Hand Sanitizer Foam (ethyl alcohol), 62% v/v, packaged in a) 1

Medline Industries Inc · Northfield, IL

Risk level
Class II
Reported by FDA
Dec 29, 2021
Recall ID
D-0287-2022
Check your lot numberHow we source this data

Summary

Medline Industries recalled Hand Sanitizer Foam starting Nov 8, 2021. The FDA classified it as Class II (temporary or reversible health risk) and published enforcement report D-0287-2022 on Dec 29, 2021. Reason: Defective Container: Customer complaints for leaking bottles and dispensing issues. Status: Terminated.

Why it was recalled

Defective Container: Customer complaints for leaking bottles and dispensing issues.

Product description

Hand Sanitizer Foam (ethyl alcohol), 62% v/v, packaged in a) 1.5 Oz. cans, NDC 53329-970-12; b) 8 Oz. (227 g) cans, NDC 53329-970-08; and c) 16 Oz. (453 g) cans, NDC 53329-970-06; Manufactured for: Medline Industries, Inc., Northfield, IL 60093.

Lot numbers, UPCs & expiration codes

Lot #: a) 32890, exp 04/2022; 33141, 33215, exp 10/2022; 33350, exp 12/2022; 33461, exp 03/2023; b) 32858, exp 02/2022; 32889, exp 03/2022; 32968, 32977, 32975, 32984, exp 06/2022; 33294, 33295, 33322, 33323, exp 12/2022; 33384, exp 01/2023; Lot 33620, exp 07/2023; c) 32728, exp 10/2021; 32859, 32889, exp 03/2022; 32985, 32988, 33004, exp 06/2022; 33339, exp 12/2022; 33501, exp 03/2023; 33502, exp 04/2023; 33621, 33622, exp 07/2023

Where it was sold

Nationwide in the USA, Canada, Hong Kong, and Peru

What to do if you have this product

  • Compare the lot number and expiration date on your package with the codes above.
  • Don't stop taking a prescription medicine on your own. Call your pharmacist or doctor; they can confirm whether your supply is affected and arrange a replacement.
  • If you have symptoms you think are related, contact your doctor. In an emergency call 911.
  • Report side effects to FDA MedWatch at 1-800-FDA-1088.

Recall details

Recall number
D-0287-2022
Classification
Class II
Status
Terminated
Recall initiated
Nov 8, 2021
FDA report date
Dec 29, 2021
Quantity
470,555 bottles
Recall type
Voluntary: Firm initiated
Recalling firm
Medline Industries Inc

Original FDA data

Every field from FDA enforcement report D-0287-2022, exactly as published.

Show all FDA fields
City
Northfield
State
IL
Status
Terminated
Country
United States
Event ID
89036
Address
3 Lakes Dr
Code information
Lot #: a) 32890, exp 04/2022; 33141, 33215, exp 10/2022; 33350, exp 12/2022; 33461, exp 03/2023; b) 32858, exp 02/2022; 32889, exp 03/2022; 32968, 32977, 32975, 32984, exp 06/2022; 33294, 33295, 33322, 33323, exp 12/2022; 33384, exp 01/2023; Lot 33620, exp 07/2023; c) 32728, exp 10/2021; 32859, 32889, exp 03/2022; 32985, 32988, 33004, exp 06/2022; 33339, exp 12/2022; 33501, exp 03/2023; 33502, exp 04/2023; 33621, 33622, exp 07/2023
Postal code
60093-2753
Report date
Dec 29, 2021
Product type
Drugs
Recall number
D-0287-2022
Classification
Class II
Recalling firm
Medline Industries Inc
Product quantity
470,555 bottles
Termination date
Aug 28, 2024
Reason for recall
Defective Container: Customer complaints for leaking bottles and dispensing issues.
Voluntary / mandated
Voluntary: Firm initiated
Product description
Hand Sanitizer Foam (ethyl alcohol), 62% v/v, packaged in a) 1.5 Oz. cans, NDC 53329-970-12; b) 8 Oz. (227 g) cans, NDC 53329-970-08; and c) 16 Oz. (453 g) cans, NDC 53329-970-06; Manufactured for: Medline Industries, Inc., Northfield, IL 60093.
Distribution pattern
Nationwide in the USA, Canada, Hong Kong, and Peru
Recall initiation date
Nov 8, 2021
Initial firm notification
Letter
Center classification date
Dec 17, 2021

How we source this data

Source: U.S. Food and Drug Administration enforcement report D-0287-2022, published Dec 29, 2021. View the source record (openFDA) · FDA enforcement reports

Last checked against FDA data: . Content last changed: .

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