Reported May 24, 2023 · Terminated

LORazepam Injection, 2mg / mL Single Dose vial 1ml vial, Rx Only, MFG Akorn Lake Forest IL 60045, Repackaged by:…

RemedyRepack Inc.

Moderate riskThis product could cause temporary or reversible health problems — stop using it.

What you should do

Stop using the affected lot and contact the recalling firm for the return or refund process. Check the FDA enforcement report for lot-level detail.

Firm contact: RemedyRepack Inc. · 625 Kolter Dr Ste 4 · Indiana, PA · 15701-3571

Is this the product you have?

  • LORazepam Injection, 2mg / mL Single Dose vial 1ml vial, Rx Only, MFG Akorn Lake Forest IL 60045
  • Repackaged by
    • RemedyRepack Inc
    • Indiana PA 15701
    • Source NDC # 17478-0040-01
    • Remedy NDC 70518-2268-00
Lot codes and dates
  • 68 of 68 codes

    • Lot # B2169656-032223
    • B2169663-032223
    • B2169680-032223
    • B2169713-032223
    • B2109085-021423
    • B2109094-021423
    • B2049229-010623
    • B2049235-010623
    • Exp. Date 04/30/2025
    • B2049224-010623
    • B2027905-122222
    • B2027920-122222
    • B2027941-122222
    • B2027968-122222
    • B2027979-122222
    • B2027989-122222
    • B2005343-120922
    • B2005333-120922
    • Exp. Date 03/31/2025
    • B1970782-112122
    • Exp. Date 01/31/2025
    • B1878510-092922
    • Exp. Date 11/30/2024
    • B1904609-101322
    • B1866210-092222
    • Exp. Date 12/31/2024
    • B1711316-060222
    • B1711328-060222
    • Exp. Date 09/30/2024
    • B1660244-042522
    • Exp. Date 07/31/2024
    • B1660288-042522
    • B1617673-032422
    • Exp. Date 06/30/2024
    • B1617737-032422
    • B1617744-032422
    • B1563407-021422
    • B1563498-021422
    • Exp. Date 05/31/2024
    • B1539158-012822
    • B1518050-011222
    • B1498175-122921
    • Exp. Date 04/30/2024
    • B1498194-122921
    • B1455889-112621
    • B1455918-112621
    • Exp. Date 03/31/2024
    • B1455901-112621
    • B1396346-101421
    • B1383216-100721
    • Exp. Date 01/31/2024
    • B1383214-100721
    • B1353451-091721
    • B1353463-091721
    • B1353480-091721
    • B1274069-071521
    • B1274079-071521
    • B1274052-071521
    • B1234313-061721
    • B1234339-061721
Amount recalled
9,038 vials

This recall covers 3 products

The agency filed one notice per product. You are reading one of them; the other 2 are below.

Where it was sold

Why it was recalled

CGMP Deviations: Discontinuation of the Quality program by manufacturer that would assure product meet the identity, strength, quality, and purity characteristics that they are purported or represented to possess.

This product could cause temporary or reversible health problems — stop using it.

Want the full recall guide?

The guide adds the identifying codes laid out for scanning, symptoms to watch for, a timeline, and news coverage of this recall.

Free recall alerts

Get alerted about new RemedyRepack Inc. recalls

One email when a matching recall is published. No account, no cost, unsubscribe in one click.

Where this came from

Source: U.S. Food & Drug Administration (openFDA)

Read the FDA (openFDA drug enforcement) notice

Notice updated Jun 21, 2023 · Data as of Sep 19, 5:54 PM UTC

RecallNow is not a government agency. Every fact on this page is published by the FDA, USDA or CPSC and links back to their notice.