CLASS II Drug recall · Reported 16 Oct 2019 · FDA Enforcement Report

DrKids Himasal Natural Nasal Saline Solution recalled by Unipharma

Unipharma is recalling DrKids Himasal Natural Nasal Saline Solution, distributed nationwide in the US. The recall was initiated on 23 Sep 2019 and the FDA has classified it as Class II.

Check your package

Lot, batch or date codesLot: 80003 Exp. 01/31/20; 70003 Exp. 10/31/19; 70005 Exp. 11/30/19; 70006 Exp. 11/30/19
Quantity recalled456 cartons

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-0133-2020
FDA event ID
83881
Recalling firm
Unipharma, Tamarac, FL
Classification
Class II
Status
Terminated
Recall initiated
23 Sep 2019
FDA classified
9 Oct 2019
Reported
16 Oct 2019
Type
Voluntary: Firm initiated
Customers notified by
Letter
Drug class
Nasal Sprays

Timeline

23 Sep 2019Recall initiated by company
9 Oct 2019Classified by FDA+16 days
16 Oct 2019Published 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

CGMP Deviations: Recall as a precautionary measure due to potential risk of product contamination with the bacteria B. cepacia.

Product as listed by the FDA

DrKids Himasal Natural Nasal Saline Solution, packaged in Pre-measured Singe-Use Vials a) 0.5 mL Each (20 count) UPC 37030244608; b) 1.5 mL Each (20 count) UPC 370302446098, Manufactured in USA by: UNIPHARMA, LLC Tamarac, FL 33321

Where it was distributed

U.S.A. Nationwide

Nationwide

Questions about this recall

Why was it recalled?

CGMP Deviations: Recall as a precautionary measure due to potential risk of product contamination with the bacteria B. cepacia.

Which lots are affected?

Lot: 80003 Exp. 01/31/20; 70003 Exp. 10/31/19; 70005 Exp. 11/30/19; 70006 Exp. 11/30/19

Where was it sold?

U.S.A. 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 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.

Other products in this recall event

1 other product · FDA event 83881

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