CLASS II Drug recall · Reported 21 Aug 2013 · FDA Enforcement Report

Medi-First First Aid Kit, Medi-first 61 Piece Kit, Home recalled

Total Resources Intl is recalling Medi-First First Aid Kit, Medi-first 61 Piece Kit, Home, Workplace Travel, Sport, Total, distributed nationwide in the US. The recall was initiated on 9 Apr 2013 and the FDA has classified it as Class II.

Check your package

Lot, batch or date codesLot 11214-07

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-890-2013
FDA event ID
64929
Recalling firm
Total Resources Intl, City of Industry, CA
Classification
Class II
Status
Terminated
Recall initiated
9 Apr 2013
FDA classified
13 Aug 2013
Reported
21 Aug 2013
Type
Voluntary: Firm initiated
Customers notified by
E-Mail
Reason category
Potency & Assay

Timeline

9 Apr 2013Recall initiated by company
13 Aug 2013Classified by FDA+126 days
21 Aug 2013Published in enforcement report+8 days

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

Reason for recall

CGMP Deviations: The first aid kits that are subject to the voluntary recall is being initiated due to failure in stability testing of the active ingredient Benzalkonium Chloride.

Potency and specification recalls happen when a batch tests outside its approved limits for strength, purity or dissolution, which can mean the dose delivered is higher or lower than labelled.

Product as listed by the FDA

Medi-First Brand First Aid Kit, MEDI-FIRST 61 Piece Kit, Home, Workplace Travel, Sport, Total Resources International, Walnut, CA 91789

Where it was distributed

Nationwide

Nationwide

Questions about this recall

Is Medi-First First Aid Kit, Medi-first 61 Piece Kit, Home, Workplace Travel, Sport, Total recalled?

Yes. Total Resources Intl recalled Medi-First First Aid Kit, Medi-first 61 Piece Kit, Home, Workplace Travel, Sport, Total on 9 Apr 2013. The recall is Class II and its status is Terminated. Recall number D-890-2013.

Why was it recalled?

CGMP Deviations: The first aid kits that are subject to the voluntary recall is being initiated due to failure in stability testing of the active ingredient Benzalkonium Chloride.

Which lots are affected?

Lot 11214-07

Where was it sold?

Nationwide

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

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