Skip to content
Recall Observatory FDA recall evidence

Exact FDA event identifier

Event 77432

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

Open FDA event record

Event summary

Timeline bucket
May 12, 2017
Product types
Food
Classifications
Class II
Statuses
Terminated
Recalling firm wording
Nutri-Dyn Midwest, Inc.

Dossier provenance

Source snapshots represented here

  • openFDA Food 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

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.

food · product 1 of 1

Nutri-Dyn Calcium D-Glucarate Plus, Dietary Supplement, 60 Capsules, UPC 7 13757-09611 9

F-2423-2017
Recall number
F-2423-2017
Initiated
May 12, 2017
Classification
Class II
Status
Terminated
Recalling firm
Nutri-Dyn Midwest, Inc.
Quantity
856 bottles

App-derived interpretation

Unknown reason.no_named_rule · v1.0.0
During production of St. John's Wort, Lot 160876, a number of bottles were mistakenly labeled as Calcium D-Glucarate Plus

These labels are deterministic app interpretations, not FDA categories.

Inspect official wording and provenance

Reason for recall

During production of St. John's Wort, Lot 160876, a number of bottles were mistakenly labeled as Calcium D-Glucarate Plus

Code information

Lot 160876 MFG 10/16

Distribution pattern

US: AZ, CA, CO,, FL, IA, ID, MA, MD, MI, MN, MO, MT, NC, ND, NE, NJ, NV, NY, OH, PA SC, SC, TX, WI, WY. OUS: ISRAEL