Reported Aug 16, 2017 · Terminated

Neostigmine Methylsulfate Injection Solution 5 mL, 5 mg/5 mL (1 mg/mL) Single-Dose Syringe, Rx Only, Cantrell Drug…

Cantrell Drug Company

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: Cantrell Drug Company · 7321 Cantrell Rd · Little Rock, AR · 72207-4144

Is this the product you have?

  • Neostigmine Methylsulfate Injection Solution 5 mL, 5 mg/5 mL (1 mg/mL) Single-Dose Syringe, Rx Only, Cantrell Drug Company 7321 Cantrell Rd. Little Rock, AR 72207 877-666-5222, NDC 52533-046-15
Lot codes and dates
  • Lot #: 10081
  • BUD
    • 7/25/2017
    • 10096
  • BUD
    • 7/27/2017
    • 10112
  • BUD
    • 7/30/2017
    • 10117
  • BUD
    • 7/31/2017
    • 10152
  • BUD
    • 8/3/2017
    • 10159
  • BUD
    • 8/6/2017
    • 10170
  • BUD
    • 8/7/2017
    • 10174
  • BUD
    • 8/8/2017
    • 10193
  • BUD
    • 8/9/2017
    • 10202
  • BUD
    • 8/10/2017
    • 10212
  • BUD
    • 8/13/2017
    • 10242
  • BUD
    • 8/15/2017
    • 10276
  • BUD
    • 8/17/2017
    • 10294
  • BUD
    • 8/20/2017
    • 10320
  • BUD
    • 8/23/2017
    • 10328
  • BUD
    • 8/24/2017
    • 10334
  • BUD
    • 8/28/2017
    • 10342
  • BUD
    • 8/29/2017
    • 10364
  • BUD
    • 9/3/2017
    • 10392
  • BUD
    • 9/6/2017
    • 10420
  • BUD
    • 9/11/2017
    • 10427
  • BUD
    • 9/12/2017
    • 10440
  • BUD
    • 9/14/2017
    • 10463
  • BUD
    • 9/18/2017
    • 10495
  • BUD
    • 9/22/2017
    • 10499
  • BUD
    • 9/24/2017
    • 10512
  • BUD
    • 9/25/2017
    • 10556
  • BUD
    • 10/1/2017
    • 10567
  • BUD
    • 10/3/2017
    • 10583
  • BUD10/6/2017
Amount recalled
120856 syringes

This recall covers 18 products

The agency filed one notice per product. You are reading one of them; the other 17 are below.

5 more are in the archive.

Where it was sold

  • Nationwide

Why it was recalled

Lack of Sterility Assurance.

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.

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Where this came from

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

Read the FDA (openFDA drug enforcement) notice

Notice updated Sep 16, 2020 · Data as of Sep 19, 8:00 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.