CLASS II Food recall · Reported 6 Aug 2014 · FDA Enforcement Report
Chitosan, Blister Pack recalled by GM Manufacturing
GM Manufacturing is recalling Chitosan, Blister Pack, distributed in California. The recall was initiated on 3 Jul 2014 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-2274-2014
- FDA event ID
- 68717
- Recalling firm
- GM Manufacturing, Gardena, CA
- Brand
- Chitosan
- Classification
- Class II
- Status
- Terminated
- Recall initiated
- 3 Jul 2014
- FDA classified
- 31 Jul 2014
- Reported
- 6 Aug 2014
- Type
- Voluntary: Firm initiated
- Customers notified by
- Letter
- Reason category
- Manufacturing (CGMP) Deviations
- Product category
- Other
Timeline
| 3 Jul 2014 | Recall initiated by company | |
| 31 Jul 2014 | Classified by FDA | +28 days |
| 6 Aug 2014 | Published in enforcement report | +6 days |
Companies usually start a recall weeks before the FDA classifies and publishes it; the gap above is that lag.
Reason for recall
GM Manufacturing is recalling dietary supplements due to significant violations of the cGMP regulations for dietary supplements.
Product as listed by the FDA
Chitosan, Blister Pack
Where it was distributed
CA
Questions about this recall
Is Chitosan, Blister Pack recalled?
Yes. GM Manufacturing recalled Chitosan, Blister Pack on 3 Jul 2014. The recall is Class II and its status is Terminated. Recall number F-2274-2014.
Why was it recalled?
GM Manufacturing is recalling dietary supplements due to significant violations of the cGMP regulations for dietary supplements.
Which lots are affected?
7/9/12 > 7/11/12
Where was it sold?
CA
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 21 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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