CLASS II Food recall · Reported 26 Jun 2019 · FDA Enforcement Report

DPS Throat Spray recalled by APS BioGroup

APS BioGroup is recalling DPS Throat Spray, distributed nationwide in the US. The recall was initiated on 15 May 2019 and the FDA has classified it as Class II.

Check your package

Lot, batch or date codesManufactured April 21, 2019. Lot 9068-2, Item # 4044, Bulk # UL-7, Exp. Date 04/2021; Lot 9068-3, Item # 4691, Bulk # UL-7, Exp. Date 04/2021; Lot 9068-4, Item # 4181, Bulk # UL-7, Exp. Date 04/2021; Lot 9068-5, Item # 00064, Bulk # UL-7, Exp. Date 04/2021; Lot 9068-6, Item # 00064, Bulk # UL-7, Exp. Date 04/2021
Quantity recalled7,132 Total Units

Do not eat it. Return it to the store for a refund or throw it away. If you have symptoms after eating it, contact a doctor.

Recall details

Recall number
F-1480-2019
FDA event ID
82900
Recalling firm
APS BioGroup, Phoenix, AZ
Classification
Class II
Status
Terminated
Recall initiated
15 May 2019
FDA classified
18 Jun 2019
Reported
26 Jun 2019
Type
Voluntary: Firm initiated
Customers notified by
Two or more of the following: Email, Fax, Letter, Press Release, Telephone, Visit
Reason category
Other Reasons
Product category
Other

Timeline

15 May 2019Recall initiated by company
18 Jun 2019Classified by FDA+34 days
26 Jun 2019Published 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

The recall is being conducted as a result of elevated APC levels. Through additional testing, it was determined that the organism is Stenotrophomonas maltophilia.

Product as listed by the FDA

DPS Throat Spray, UPC 8 55602 00021 3. Colostrum Immune Concentrate. Net 150 ml

Where it was distributed

Nationwide and Switzerland. No military/govt/VA consignees.

Nationwide Virginia

Questions about this recall

Is DPS Throat Spray recalled?

Yes. APS BioGroup recalled DPS Throat Spray on 15 May 2019. The recall is Class II and its status is Terminated. Recall number F-1480-2019.

Why was it recalled?

The recall is being conducted as a result of elevated APC levels. Through additional testing, it was determined that the organism is Stenotrophomonas maltophilia.

Which lots are affected?

Manufactured April 21, 2019. Lot 9068-2, Item # 4044, Bulk # UL-7, Exp. Date 04/2021; Lot 9068-3, Item # 4691, Bulk # UL-7, Exp. Date 04/2021; Lot 9068-4, Item # 4181, Bulk # UL-7, Exp. Date 04/2021; Lot 9068-5, Item # 00064, Bulk # UL-7, Exp. Date 04/2021; Lot 9068-6, Item # 00064, Bulk # UL-7, Exp. Date 04/2021

Where was it sold?

Nationwide and Switzerland. No military/govt/VA consignees.

What should I do if I have it?

Do not eat it. Return it to the store for a refund or throw it away. If you have symptoms after eating it, contact a doctor.

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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