Severity
Moderate
ModerateClass IITerminated
FDA Food recall · Reported August 6, 2014
DMSA, 100cc HDPE bottle
GM Manufacturing is recalling dietary supplements due to significant violations of the cGMP regulations for dietary supplements.
Gm Manufacturing Inc. recalled DMSA, 100cc HDPE bottle - a moderate-severity action.
DMSA, 100cc HDPE bottle was recalled by Gm Manufacturing Inc. in August 6, 2014. Reason: GM Manufacturing is recalling dietary supplements due to significant violations of the cGMP regulations for d…. Check the official notice for the remedy. Verify recall #F-2266-2014 with the FDA Food before acting.
The recall
Gm Manufacturing Inc. issued this moderate-severity FDA Food recall-GM Manufacturing is recalling dietary supplements due to significant violations of the cGMP regulations for d….
- Moderate
- severity level
- 414 units
- affected scope
- Class II
- classification
- August 6, 2014
- reported
Sourced from official FDA Food enforcement records. Verify recall #F-2266-2014 with the agency before acting. Full product description, hazard, remedy, and related recalls are below.
Recall Insight
This FDA Food action (record #F-2266-2014) was formally reported on August 6, 2014, with the manufacturer initiating the action on July 3, 2014. It is classified under Moderate severity (Class II), with a current status of Terminated. Gm Manufacturing Inc. is listed as the recalling firm, operating out of Gardena, CA. Federal records list the affected scope as 414 units.
The documented reason for this recall is: GM Manufacturing is recalling dietary supplements due to significant violations of the cGMP regulations for dietary supplements. Distribution data in the federal record shows the product reached: CA. Distribution scope directly affects the consumer exposure window and determines whether a recall remains regional or escalates into a nationwide advisory.
Within the same product category the archive holds 6 closely related recalls - clustering in a narrow category often points to a systemic quality-control or supplier issue rather than a one-off defect. Always verify the recall number against the official agency record before acting.
Children & Baby Products recalls over time
Where this recall sits in its category - 3,731 children & baby products recalls on record
Of 101,704 recalls in the database, 24,878 are high severity, 72,426 moderate, and 4,400 low. This recall is classified moderate severity.
Counts reflect market size and reporting activity, not inherent danger, we do not rank products by risk from raw recall volume.
Affected scope
414 units
Related Recalls
6
0 from same agency
Product description
DMSA, 100cc HDPE bottle
Reason for recall
GM Manufacturing is recalling dietary supplements due to significant violations of the cGMP regulations for dietary supplements.
Recall Profile
| Attribute | Value |
|---|---|
| Agency | U.S. Food and Drug Administration |
| Severity class | Moderate (Class II) |
| Status | Terminated |
| Recall number | F-2266-2014 |
| Date reported | August 6, 2014 |
| Date initiated | July 3, 2014 |
| Recalling firm | Gm Manufacturing Inc. |
| Firm location | Gardena, CA |
| Affected scope | 414 units |
| Distribution | CA |
Profile values are sourced directly from the official FDA Food enforcement record. Source: U.S. Food and Drug Administration.
What to do with this recall
Match your product against the recall record, then act on the agency remedy.
- Check the recall number (F-2266-2014) and product description against the item you own. Search the archive
- Confirm the current status with FDA Food before acting, recall details can be updated.
- Follow the documented remedy (refund, replacement, repair, or disposal) rather than general advice. What to do next
This page summarizes the official FDA Food record for research and awareness; it is not legal, medical, or safety advice. Verify with the issuing agency before acting.
Frequently Asked Questions
What product was recalled? ▼
DMSA, 100cc HDPE bottle. Recalled by Gm Manufacturing Inc.. Units affected: 414 units.
Why was this product recalled? ▼
GM Manufacturing is recalling dietary supplements due to significant violations of the cGMP regulations for dietary supplements.
Which agency issued this recall? ▼
This recall was issued by the FDA Food on August 6, 2014. Severity: Moderate. Recall number: F-2266-2014.
Where was the recalled product distributed? ▼
Distribution: CA.
How do I check if my product is affected by a recall? ▼
Check the product description and recall number (F-2266-2014) against your product. Visit the official FDA Food website for the most current information. You can also use our Recall Checker tool to search by product name or brand.
What are the health risks of consuming a recalled food product? ▼
Recalled food products may contain contaminants, undeclared allergens, or harmful bacteria such as Salmonella, Listeria, or E. coli. Consuming these products can cause foodborne illness ranging from mild gastrointestinal symptoms to serious conditions requiring hospitalization. If you have consumed a recalled food product and experience symptoms, contact your healthcare provider and report to the FDA via MedWatch.
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Every figure on PlainRecalls is rendered directly from official FDA, CPSC and NHTSA recall records, no number is typed in by an editor. This recall: FDA Food, reported August 6, 2014. Severity classes follow each agency's own taxonomy (FDA Class I/II/III; CPSC and NHTSA by hazard type), and related-recall context is computed across the full archive. See our editorial standards & corrections policy, the methodology behind these numbers, or report a data error. Data current as of July 2026.