Severity
Low
FDA Food recall · Reported June 1, 2016
ZoChem Inc. received a complaint from a customer who noticed black specs of contamination in one specific lot (#700792) of product (zinc oxide) that they received, an investigati…
Zochem Inc. recalled Zinc Oxide Powder (API) used in the manufacturing of dietary supplements . - a low-severity action.
Zinc Oxide Powder (API) used in the manufacturing of dietary supplements . was recalled by Zochem Inc. in June 1, 2016. Reason: ZoChem Inc. received a complaint from a customer who noticed black specs of contamination in one specific lo…. Check the official notice for the remedy. Verify recall #F-1402-2016 with the FDA Food before acting.
The recall
Zochem Inc. issued this low-severity FDA Food recall-ZoChem Inc. received a complaint from a customer who noticed black specs of contamination in one specific lo….
Sourced from official FDA Food enforcement records. Verify recall #F-1402-2016 with the agency before acting. Full product description, hazard, remedy, and related recalls are below.
This FDA Food action (record #F-1402-2016) was formally reported on June 1, 2016, with the manufacturer initiating the action on March 11, 2016. It is classified under Low severity (Class III), with a current status of Terminated. Zochem Inc. is listed as the recalling firm, operating out of Brampton, N/A. Federal records list the affected scope as (Lot # 700785 & 700804) of 19200 lbs each (total 38400 lbs) , lot (LOT#700792) of 450 kg was made and distributed.
The documented reason for this recall is: ZoChem Inc. received a complaint from a customer who noticed black specs of contamination in one specific lot (#700792) of product (zinc oxide) that they received, an investigation by ZoChem Inc. was launched . … Distribution data in the federal record shows the product reached: (2) lots (Lot # 700785 & 700804) of 19200 lbs each (total 38400 lbs) were made and distributed to Brand Nu Laboratories (distributor) at the following address: 377 Research Parkway, Meriden, CT 06450. One (1) lot (…. 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, 6 from FDA Food - 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.
Where this recall sits in its category - 2,002 dietary supplements 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 low severity.
Counts reflect market size and reporting activity, not inherent danger, we do not rank products by risk from raw recall volume.
Severity
Low
Affected scope
(Lot # 700785 & 700804) of 19200 lbs each (total 38400 lbs) , lot (LOT#700792) of 450 kg was made and distributed
Related Recalls
6
6 from same agency
Zinc Oxide Powder (API) used in the manufacturing of dietary supplements .
ZoChem Inc. received a complaint from a customer who noticed black specs of contamination in one specific lot (#700792) of product (zinc oxide) that they received, an investigation by ZoChem Inc. was launched . The retained sample representing this lot was analyzed and the contaminant was determined to be iron. The issue is potentially present in two other lots (#700785 & 700804) produced
| Attribute | Value |
|---|---|
| Agency | U.S. Food and Drug Administration |
| Severity class | Low (Class III) |
| Status | Terminated |
| Recall number | F-1402-2016 |
| Date reported | June 1, 2016 |
| Date initiated | March 11, 2016 |
| Recalling firm | Zochem Inc. |
| Firm location | Brampton, N/A |
| Affected scope | (Lot # 700785 & 700804) of 19200 lbs each (total 38400 lbs) , lot (LOT#700792) of 450 kg was made and distributed |
| Distribution | (2) lots (Lot # 700785 & 700804) of 19200 lbs each (total 38400 lbs) were made and distributed to Brand Nu Laboratories (distributor) at the following address: 377 Research Parkway, Meriden, CT 06450. One (1) lot (LOT#700792) of 450 k… |
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.
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.
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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 June 1, 2016. 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.