Reported Aug 16, 2017 · Terminated
Norepinephrine Bitartrate 8 mg Added to 0.9% Sodium Chloride 250 mL (32 mcg per mL) Single-Dose Bag, Rx Only, Cantrell…
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?
- Norepinephrine Bitartrate 8 mg Added to 0.9% Sodium Chloride 250 mL (32 mcg per mL) Single-Dose Bag, Rx Only, Cantrell Drug Company 7321 Cantrell Rd. Little Rock, AR 72207 877-666-5222, NDC 52533-217-18
- Lot codes and dates
- Lot #: 10095
- BUD
7/27/201710119
- BUD
7/31/201710135
- BUD
8/2/201710162
- BUD
8/6/201710168
- BUD
8/7/201710186
- BUD
8/9/201710247
- BUD
8/15/201710301
- BUD
8/21/201710325
- BUD
8/24/201710390
- BUD
9/5/201710465
- BUD
9/18/201710487
- BUD
9/20/201710542
- BUD9/27/2017
- Amount recalled
- 8928 bags
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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