Reported Jul 27, 2016 · Terminated

2 mcg/mL Fentanyl Citrate and 0.25% Bupivacaine HCl (Preservative Free) in 0.9% Sodium Chloride, 100 mL in 150 mL…

Pharmedium Services, LLC

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: Pharmedium Services, LLC · 150 N Field Dr Ste 350 · Lake Forest, IL · 60045-2506

Is this the product you have?

  • 2 mcg/mL Fentanyl Citrate and 0.25% Bupivacaine HCl (Preservative Free) in 0.9% Sodium Chloride, 100 mL in 150 mL Baxter Intravia Bag, Service Code 2K8103, Rx Only, Compounded by PharMEDium Services, LLC, Memphis, TN 36141, NDC 61553-103-48
Lot codes and dates

18 of 18 products

Products covered by this recall
#Product as published
1Lot Number 160390174M , Exp. Date 5/9/2016
2Lot Number 160400196M , Exp. Date 5/10/2016
3Lot Number 160470128M , Exp. Date 5/17/2016
4Lot Number 160530287M , Exp. Date 5/23/2016
5Lot Number 160540190M , Exp. Date 5/24/2016
6Lot Number 160590168M , Exp. Date 5/29/2016
7Lot Number 160610129M , Exp. Date 5/31/2016
8Lot Number 160680254M , Exp. Date 6/7/2016
9Lot Number 160700199M , Exp. Date 6/9/2016
10Lot Number 160750132M , Exp. Date 6/14/2016
11Lot Number 160770177M , Exp. Date 6/16/2016
12Lot Number 160810292M , Exp. Date 6/20/2016
13Lot Number 160820115M , Exp. Date 6/21/2016
14Lot Number 160840157M , Exp. Date 6/23/2016
15Lot Number 160880249M , Exp. Date 6/27/2016
16Lot Number 160890261M , Exp. Date 6/28/2016
17Lot Number 160940057M , Exp. Date 7/2/2016
18Lot Number 160960151M , Exp. Date 7/5/2016
Amount recalled
425 bags

This recall covers 75 products

The agency filed one notice per product. You are reading one of them; the other 74 are below.

62 more are in the archive.

Where it was sold

  • Nationwide

Why it was recalled

Presence of Particulate Matter: API contaminated with glass particulate was used to produce sterile injectable drugs.

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

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Where this came from

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

Read the FDA (openFDA drug enforcement) notice

Notice updated Mar 6, 2018 · Data as of Sep 19, 4:59 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.