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Class II: temporary or reversible health riskTerminated

Vi-Jon 70% ISOPROPYL ALCOHOL First aid antiseptic Recall

70% ISOPROPYL ALCOHOL First aid antiseptic, 4 FL OZ (118 mL) bottle, Made in US with US…

Vi-Jon, LLC · Smyrna, TN

Risk level
Class II
Reported by FDA
Jun 29, 2022
Recall ID
D-1151-2022
Check your lot numberHow we source this data

Summary

Vi-Jon recalled 70% ISOPROPYL ALCOHOL First aid antiseptic starting Jun 15, 2022. The FDA classified it as Class II (temporary or reversible health risk) and published enforcement report D-1151-2022 on Jun 29, 2022. Reason: Defective Container: Product may leak when squeezed or when not in an upright position determined to be due to defects in the bottle neck finish and insufficient tightening. Status: Terminated.

Why it was recalled

Defective Container: Product may leak when squeezed or when not in an upright position determined to be due to defects in the bottle neck finish and insufficient tightening.

Product description

70% ISOPROPYL ALCOHOL First aid antiseptic, 4 FL OZ (118 mL) bottle, Made in US with US and foreign components for Medline Industries, Inc., Mundelein, IL 60060 USA, NDC: 53329-798-04, UPC (01) 10888277362291.

Lot numbers, UPCs & expiration codes

Lots #s: 0517418, Exp. 12/2022; 0506632, 0519195, 0522494, Exp. 01/2023; 0525627, 0525629, 0526051, 0526052, 0527664, 0527665, Exp. 03/2023; 0531133, 0531134, Exp. 04/2023; 0533153, 0534050, Exp. 05/2023; 0534585, 0534587, 0536089, Exp. 06/2023; 0538694, 0541334, Exp. 07/2023; 0539877, 0542355, Exp. 08/2023; 0545225, 0547054, 0547055, 0547131, Exp. 09/2023; 0547130, 0551014, 0551015, 0552608, Exp. 10/2023; 0552609, 0552610, 0553905, Exp. 11/2023; 0556144, 0557513, Exp. 12/2023; 0559594, 0559602, 0559603, Exp. 01/2024; 0551013, 0559596, 0559604, 0559605, 0561393, 0561395, Exp. 02/2024; 0556143, 0561396, 0561549, Exp. 03/2024; 0565877, Exp. 04/2024

Where it was sold

Nationwide in the USA

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-1151-2022
Classification
Class II
Status
Terminated
Recall initiated
Jun 15, 2022
FDA report date
Jun 29, 2022
Quantity
3,157,620 bottles
Recall type
Voluntary: Firm initiated
Recalling firm
Vi-Jon, LLC

Original FDA data

Every field from FDA enforcement report D-1151-2022, exactly as published.

Show all FDA fields
City
Smyrna
State
TN
Status
Terminated
Country
United States
Event ID
90453
Address
1 Swan Dr
Code information
Lots #s: 0517418, Exp. 12/2022; 0506632, 0519195, 0522494, Exp. 01/2023; 0525627, 0525629, 0526051, 0526052, 0527664, 0527665, Exp. 03/2023; 0531133, 0531134, Exp. 04/2023; 0533153, 0534050, Exp. 05/2023; 0534585, 0534587, 0536089, Exp. 06/2023; 0538694, 0541334, Exp. 07/2023; 0539877, 0542355, Exp. 08/2023; 0545225, 0547054, 0547055, 0547131, Exp. 09/2023; 0547130, 0551014, 0551015, 0552608, Exp. 10/2023; 0552609, 0552610, 0553905, Exp. 11/2023; 0556144, 0557513, Exp. 12/2023; 0559594, 0559602, 0559603, Exp. 01/2024; 0551013, 0559596, 0559604, 0559605, 0561393, 0561395, Exp. 02/2024; 0556143, 0561396, 0561549, Exp. 03/2024; 0565877, Exp. 04/2024
Postal code
37167-2099
Report date
Jun 29, 2022
Product type
Drugs
Recall number
D-1151-2022
Classification
Class II
Recalling firm
Vi-Jon, LLC
Product quantity
3,157,620 bottles
Termination date
Jul 5, 2024
Reason for recall
Defective Container: Product may leak when squeezed or when not in an upright position determined to be due to defects in the bottle neck finish and insufficient tightening.
Voluntary / mandated
Voluntary: Firm initiated
Product description
70% ISOPROPYL ALCOHOL First aid antiseptic, 4 FL OZ (118 mL) bottle, Made in US with US and foreign components for Medline Industries, Inc., Mundelein, IL 60060 USA, NDC: 53329-798-04, UPC (01) 10888277362291.
Distribution pattern
Nationwide in the USA
Recall initiation date
Jun 15, 2022
Initial firm notification
Letter
Center classification date
Jun 21, 2022

How we source this data

Source: U.S. Food and Drug Administration enforcement report D-1151-2022, published Jun 29, 2022. View the source record (openFDA) · FDA enforcement reports

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

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