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Syntho Pharmaceuticals, Inc. recalls

Every recall we track for Syntho Pharmaceuticals, Inc. — 2 in all, all from 2017 — plus the complaints and injury reports the public filed about them.

2recalls

Recalls per year, by danger level

2 recalls since 2017.

2017: 2 recalls — 1 lower risk, 1 not yet rated220172018: 0 recalls20182019: 0 recalls20192020: 0 recalls20202021: 0 recalls20212022: 0 recalls20222023: 0 recalls20232024: 0 recalls20242025: 0 recalls20252026 (to date): 0 recalls2026to date

All FDA recall records for Syntho Pharmaceuticals, Inc. since 2017, counted by recall date (one bar per calendar year; 2026 is partial). Danger level is GovInfoNow’s plain-language rating; “not yet rated” records are still being written up.

Recalls per year for Syntho Pharmaceuticals, Inc., by danger level
YearStop using nowUse cautionLower riskNot yet ratedTotal
201700112
201800000
201900000
202000000
202100000
202200000
202300000
202400000
202500000
2026 (to date)00000

Most common reasons for Syntho Pharmaceuticals, Inc. recalls

  • CGMP deviations: Lots were recalled due to sub-potency and cGMP violations.2

What to do if you have a recalled Syntho Pharmaceuticals, Inc. product

  1. Match the NDC and lot number on your bottle or box to the recall.
  2. Don’t stop a prescription on your own — ask your pharmacist or doctor for a replacement first.
  3. Report side effects to FDA MedWatch.

See this week’s new recalls.

All Syntho Pharmaceuticals, Inc. recalls

1 shown

Syntho Pharmaceuticals, Inc. recall questions

How many recalls has Syntho Pharmaceuticals, Inc. had?

2 recalls from Syntho Pharmaceuticals, Inc. are on record with U.S. safety agencies, from 2017.

What is the most recent Syntho Pharmaceuticals, Inc. recall?

Syntho Pharmaceuticals, Inc. recalls EEMT HS (esterified estrogens and methyltestosterone) 0.625 mg/1.25 mg, tablets,100-count bottle, Rx only, Manufactured, dated Apr 17, 2017. Every Syntho Pharmaceuticals, Inc. recall is listed on this page, newest first.

Why are Syntho Pharmaceuticals, Inc. products recalled?

The most common reasons on record: CGMP deviations: Lots were recalled due to sub-potency and cGMP violations. (2).

What should I do if I have a recalled Syntho Pharmaceuticals, Inc. 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 Syntho Pharmaceuticals, Inc. 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.