Monarch PCM Ferretts IPS Iron Liquid Recall: Stability Issue
Monarch PCM recalls Ferretts IPS Iron Liquid Dietary Supplement due to stability problems affecting product safety. Learn about affected items and what to do.
Lower-risk recall
Stability is out of spec at 81% for 3 month time period.
Contact the company
What happened, in plain English
Monarch PCM is recalling Ferret:ts IPS Iron Liquid Dietary Supplement because it may not stay stable for the claimed 3-month period. This could lead to potential safety issues with the iron supplement. Read more at govinfonow.com/recall/14172-monarch-pcm-ferretts-ips-iron-liquid-recall-stability-issue.
Source Summary by GovInfoNow · govinfonow.com/recall/14172-monarch-pcm-ferretts-ips-iron-liquid-recall-stability-issue · Updated October 4, 2026 · FDA enforcement record: FDA #F-1020-2021
Cite this page
“Monarch PCM Ferretts IPS Iron Liquid Recall: Stability Issue.” GovInfoNow, updated October 4, 2026. https://govinfonow.com/recall/14172-monarch-pcm-ferretts-ips-iron-liquid-recall-stability-issue. Based on FDA recall #F-1020-2021 (https://api.fda.gov/food/enforcement.json?search=recall_number:%22F-1020-2021%22&limit=1).
Why it’s dangerous
The product's stability is out of spec at 81% for a 3-month time period. This means the iron supplement may not maintain its intended quality over time, potentially leading to safety concerns.
Who’s affected
People who purchased the Ferretts IPS Iron Liquid Dietary Supplement from Monarch PCM are affected. Those with dietary needs for iron supplementation are most at risk.
How to tell if you have this one
Check for the Ferretts IPS Iron Liquid Dietary Supplement with a white round bottle labeled 8 oz. (15 mL) and lot number 21FP1658.
- Brand
Monarch PCM- Category
Food
What to do — step by step
Check Product Details
Look for the white round bottle labeled 8 oz. (15 mL) with lot number 21FP1658.
Where it went and when
Where it was distributed
Distributed in Utah.
FDA distribution: “UT” States read from FDA’s own wording; “not listed” means the notice does not name it.
States: Utah.
Recall timeline
FDA terminated this recall 2.2 years after the firm started it.
- Firm started the recall
- FDA classified it Class II
- Published in FDA’s Enforcement Report
- FDA terminated the recall
Dates from the agency record only; steps without a date are left out.
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Where this comes from
The facts (hazard, remedy, dates, manufacturer) are pulled from the official FDA recall record. The plain-language summary and step-by-step checklist are written by GovInfoNow to make the official notice easier to act on — they don’t replace it.
- Official source: FDA Recall #F-1020-2021 (September 2, 2021) — FDA publishes no per-recall page; this is the official machine-readable enforcement record. Search FDA recalls for F-1020-2021 to see it in context.
- Plain-language summary written by qwen3:4b on October 4, 2026, from the official record above. Not reviewed by a person — if it conflicts with the FDA notice, the notice is correct. Report an error on this page.
- GovInfoNow is an independent service and is not a government agency. We republish official FDA recall data; we don’t issue, amend or administer recalls.