Reported Aug 16, 2017 · Terminated
Sodium Bicarbonate 8.4% Injection Solution 50 mL, 50 mEq (1mEq/mL) Single-Dose Syringe, Rx Only, Cantrell Drug Company…
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?
- Sodium Bicarbonate 8.4% Injection Solution 50 mL, 50 mEq (1mEq/mL) Single-Dose Syringe, Rx Only, Cantrell Drug Company 7321 Cantrell Rd. Little Rock, AR 72207 877-666-5222
- Lot codes and dates
- Lot#: 10349
- BUD
7/30/201710356
- BUD
7/31/201710377
- BUD
8/4/201710386
- BUD
8/5/201710394
- BUD
8/6/201710404
- BUD
8/8/201710423
- BUD
8/12/201710468
- BUD
8/18/201710473
- BUD
8/19/201710482
- BUD
8/20/201710514
- BUD
8/25/201710524
- BUD
8/26/201710569
- BUD9/3/2017
- Amount recalled
- 40081 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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