CLASS II Food recall · Reported 6 Oct 2021 · FDA Enforcement Report
Ferretts IPS Iron Liquid Dietary Supplement Iron Protein recalled
Monarch PCM is recalling Ferretts IPS Iron Liquid Dietary Supplement Iron Protein Succinylate 40 mg (elemental, distributed in Utah. The recall was initiated on 2 Sep 2021 and the FDA has classified it as Class II.
Check your package
Do not eat it. Return it to the store for a refund or throw it away. If you have symptoms after eating it, contact a doctor.
Recall details
- Recall number
- F-1020-2021
- FDA event ID
- 88597
- Recalling firm
- Monarch PCM, Fort Worth, TX
- Brand
- Ferretts IPS
- Classification
- Class II
- Status
- Terminated
- Recall initiated
- 2 Sep 2021
- FDA classified
- 27 Sep 2021
- Reported
- 6 Oct 2021
- Type
- Voluntary: Firm initiated
- Customers notified by
- Telephone
- Reason category
- Potency & Assay
- Product category
- Dietary Supplements
Timeline
| 2 Sep 2021 | Recall initiated by company | |
| 27 Sep 2021 | Classified by FDA | +25 days |
| 6 Oct 2021 | Published in enforcement report | +9 days |
Companies usually start a recall weeks before the FDA classifies and publishes it; the gap above is that lag.
Reason for recall
Stability is out of spec at 81% for 3 month time period.
Potency and specification recalls happen when a batch tests outside its approved limits for strength, purity or dissolution, which can mean the dose delivered is higher or lower than labelled.
Product as listed by the FDA
Ferretts IPS Iron Liquid Dietary Supplement Iron Protein Succinylate 40 mg (elemental iron) / 15 mL 8 oz. White Round PET 24/410 bottle
Where it was distributed
UT
Questions about this recall
Why was it recalled?
Stability is out of spec at 81% for 3 month time period.
Which lots are affected?
Finished Product Lot # 21FP1658
Where was it sold?
UT
What should I do if I have it?
Do not eat it. Return it to the store for a refund or throw it away. If you have symptoms after eating it, contact a doctor.
What does Class II mean?
Class II means the product may cause temporary or medically reversible health problems, or the probability of serious harm is remote.
Read the official FDA notice · Source record retrieved 26 Sep 2026. The FDA describes openFDA data as unvalidated; the official notice takes precedence. This page reports the record and gives no medical advice.
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