Exact FDA event identifier

Event 74888

1 recalled-product record grouped only because every row carries this exact official event ID.

Event summary

Timeline bucket: August 01, 2016
Product types: Drug
Classifications: Class II
Statuses: Terminated
Recalling firm wording: Spectrum Laboratory Products, Inc.

Dossier provenance

Source snapshots represented here

openFDA Drug Enforcement Report-date coverage June 20, 2012–July 08, 2026 Known gap: openFDA describes 2004-present coverage, but the current export has no report-date records in this interval.

Enforcement coverage uses report dates; product initiation dates can precede those bounds. Device-enrichment coverage uses FDA event_date_initiated.

How coverage and grouping work

Device root-cause evidence is not applicable to this event. No grouped product has the official product type device; this is not an unavailable-enrichment finding.

Complete imported group

Every recalled product in this event

1 official enforcement rows

Product dates, classifications, firms, and source wording remain attached to their individual rows. Opening this dossier never hides products that did not match a prior timeline filter.

drug · product 1 of 1

Zinc Acetate, Crystal, USP, packaged in 500 gram bottles, Spectrum Chemical MFG, CORP., New Brunswick, NJ 08901

D-1456-2016

Recall number: D-1456-2016
Initiated: August 01, 2016
Classification: Class II
Status: Terminated
Recalling firm: Spectrum Laboratory Products, Inc.
Quantity: 14,000 grams

App-derived interpretation

Unknown reason.no_named_rule · v1.0.0

Does not meet monograph: product exhibits lead levels in excess of the USP monograph limits.

These labels are deterministic app interpretations, not FDA categories.

Inspect official wording and provenance

Reason for recall

Does not meet monograph: product exhibits lead levels in excess of the USP monograph limits.

Code information

Lot # 2EH0257

Distribution pattern

US: MA, TN, GA, MO and Canada