CLASS II Drug recall · Reported 28 Jun 2017 · FDA Enforcement Report

Magnesium Citrate Saline Laxative Cherry Flavored recalled by Vi-Jon

Vi-Jon is recalling Magnesium Citrate Saline Laxative Cherry Flavored, distributed nationwide in the US. The recall was initiated on 12 Jun 2017 and the FDA has classified it as Class II.

Check your package

Lot, batch or date codesLot: 0313246
Quantity recalled52,212 bottles

Check the lot number on your package against the affected lots. If it matches, contact the pharmacy that dispensed it or your prescriber before stopping any medication.

Recall details

Recall number
D-0922-2017
FDA event ID
77517
Recalling firm
Vi-Jon, Smyrna, TN
Classification
Class II
Status
Terminated
Recall initiated
12 Jun 2017
FDA classified
21 Jun 2017
Reported
28 Jun 2017
Type
Voluntary: Firm initiated
Customers notified by
Letter
Reason category
Foreign Material

Timeline

12 Jun 2017Recall initiated by company
21 Jun 2017Classified by FDA+9 days
28 Jun 2017Published in enforcement report+7 days

Companies usually start a recall weeks before the FDA classifies and publishes it; the gap above is that lag.

Reason for recall

Presence of foreign substance: glass particle

Foreign material recalls cover pieces of metal, plastic, glass, wood or other objects that got into the product during processing and could cause injury if eaten.

Product as listed by the FDA

Magnesium Citrate Saline Laxative Cherry Flavored, packaged in a) 10 fl. oz. (296 mL) bottle UPC: 072785104556 (Rexall's label), b) 10 fl. oz. (296 mL) bottle UPC: 041163254138 (Equaline's label), OTC, Distributed by a) Dolgencorp, LL, Goodlettsville, TN 37072 b)Supervalu, Inc. Eden Prairie, MN 55344

Where it was distributed

Nationwide U.S.A.

Nationwide

Questions about this recall

Why was it recalled?

Presence of foreign substance: glass particle

Which lots are affected?

Lot: 0313246

Where was it sold?

Nationwide U.S.A.

What should I do if I have it?

Check the lot number on your package against the affected lots. If it matches, contact the pharmacy that dispensed it or your prescriber before stopping any medication.

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 26 Sep 2026. The FDA describes openFDA data as unvalidated; the official notice takes precedence. This page reports the record and gives no medical advice.

More recalls from Vi-Jon

All 29