Viralox
Reason The recall is being conducted as a result of elevated APC levels. Through additional testing, it was determined that the organism is Stenotrophomonas maltophilia.
Immuno PRP Spray recall
Recalled by APS BioGroup, Inc · Phoenix, AZ, United States
Class II — Moderate risk. May cause temporary or reversible harm; serious harm unlikely.
Why it was 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.
See the recall's own reason text for the specifics. All other reasons recalls.
What was recalled
Immuno PRP Spray, UPC 8 12527 01176 2. Colostrum Polypeptides. 5 fl oz (140 mL)
Quantity: 7,132 Total Units
Lot codes, dates and UPCs
A recall covers only these codes. Compare them with the lot number, best-by date or UPC printed on your package.
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 it was sold
Nationwide.
Virginia
FDA's distribution note: Nationwide and Switzerland. No military/govt/VA consignees.
Check the codes, then return or discard. Class II means eating it may cause temporary or reversible health problems. If your package matches the recalled codes, do not eat it - return it to the store or throw it away. FDA lists this recall as terminated: the company has finished removing the product, so it should no longer be on shelves - but it can still be in a freezer or pantry.
- Recalling firm
- APS BioGroup, Inc
- Initiated by
- Voluntary: Firm initiated
- Recall initiated
- May 15, 2019
- In FDA report of
- Jun 26, 2019
- Terminated
- Dec 27, 2019
- FDA recall number
- F-1478-2019 · event 82900
- Official record
- FDA enforcement report search
Also recalled with it (3 more products)
FDA files each product of one recall action separately; these share the same FDA event.
DPS Throat Spray
Reason The recall is being conducted as a result of elevated APC levels. Through additional testing, it was determined that the organism is Stenotrophomonas maltophilia.
Immulox
Reason The recall is being conducted as a result of elevated APC levels. Through additional testing, it was determined that the organism is Stenotrophomonas maltophilia.