Amerita Specialty Infusion Services recalls
Every recall we track for Amerita Specialty Infusion Services — 2 in all, all from 2015 — plus the complaints and injury reports the public filed about them. 1 is rated “stop using now”.
Most common reasons for Amerita Specialty Infusion Services recalls
What to do if you have a recalled Amerita Specialty Infusion Services product
- Match the NDC and lot number on your bottle or box to the recall.
- Don’t stop a prescription on your own — ask your pharmacist or doctor for a replacement first.
- Report side effects to FDA MedWatch.
All Amerita Specialty Infusion Services recalls
1 shownAmerita Specialty Infusion Services recall questions
How many recalls has Amerita Specialty Infusion Services had?
2 recalls from Amerita Specialty Infusion Services are on record with U.S. safety agencies, from 2015.
What is the most recent Amerita Specialty Infusion Services recall?
Amerita Specialty Infusion Services recalls IT Custom Compound (BC) Baclofen 2000 mcg/ml, Clonidine 2 mcg/ml 40 ml PF syringe, FOR INTRATHECAL USE ONLY, Rx Only,, dated Dec 24, 2015. Every Amerita Specialty Infusion Services recall is listed on this page, newest first.
Why are Amerita Specialty Infusion Services products recalled?
The most common reasons on record: Lack of Assurance of Sterility (2).
What should I do if I have a recalled Amerita Specialty Infusion Services product?
Match the NDC and lot number on your bottle or box to the recall. Don’t stop a prescription on your own — ask your pharmacist or doctor for a replacement first. Report side effects to FDA MedWatch.
How do I get alerts for new Amerita Specialty Infusion Services recalls?
Sign up for free email alerts on GovInfoNow — we check official CPSC, FDA, USDA and NHTSA data every day and email you only when a recall matches what you follow.