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ULTRAtab Laboratories, Inc. recalls

Every recall we track for ULTRAtab Laboratories, Inc. — 43 in all, from 2021–2022 — plus the complaints and injury reports the public filed about them.

43recalls

Recalls per year, by danger level

Recalls from ULTRAtab Laboratories, Inc. peaked in 2022 (33); 43 since 2017.

2017: 0 recalls20172018: 0 recalls20182019: 0 recalls20192020: 0 recalls20202021: 10 recalls — 1 use caution, 5 lower risk, 4 not yet rated1020212022: 33 recalls — 5 lower risk, 28 not yet rated3320222023: 0 recalls20232024: 0 recalls20242025: 0 recalls20252026 (to date): 0 recalls2026to date

All FDA recall records for ULTRAtab Laboratories, 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 ULTRAtab Laboratories, Inc., by danger level
YearStop using nowUse cautionLower riskNot yet ratedTotal
201700000
201800000
201900000
202000000
2021015410
20220052833
202300000
202400000
202500000
2026 (to date)00000

Most common reasons for ULTRAtab Laboratories, Inc. recalls

  • CGMP Deviations33
  • cGMP Deviations9

What to do if you have a recalled ULTRAtab Laboratories, 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 ULTRAtab Laboratories, Inc. recalls

3 shown

ULTRAtab Laboratories, Inc. recall questions

How many recalls has ULTRAtab Laboratories, Inc. had?

43 recalls from ULTRAtab Laboratories, Inc. are on record with U.S. safety agencies, from 2021–2022 (34 drug, 9 food).

What is the most recent ULTRAtab Laboratories, Inc. recall?

ULTRAtab Laboratories, Inc. recalls APAP 500 mg tablet (Acetaminophen 500 mg) Bulk Container, ULTRAtab Laboratories, Inc., Highland, NY NDC 62959-210-00, dated Jan 26, 2022. Every ULTRAtab Laboratories, Inc. recall is listed on this page, newest first.

Why are ULTRAtab Laboratories, Inc. products recalled?

The most common reasons on record: CGMP Deviations (33); cGMP Deviations (9).

What should I do if I have a recalled ULTRAtab Laboratories, 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 ULTRAtab Laboratories, 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.