CLASS I Food recall · Reported 21 Feb 2018 · FDA Enforcement Report

Zero for Him recalled by ABH Nature's Products

ABH Nature's Products is recalling Zero for Him, distributed in Massachusetts, Pennsylvania. The recall was initiated on 20 Jan 2018 and the FDA has classified it as Class I.

Check your package

Lot, batch or date codesLot#1710638B
Quantity recalled1,137 bottles

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-0813-2018
FDA event ID
78983
Recalling firm
ABH Nature's Products, Edgewood, NY
Brand
Zero
Classification
Class I
Status
Terminated
Recall initiated
20 Jan 2018
FDA classified
15 Feb 2018
Reported
21 Feb 2018
Type
Voluntary: Firm initiated
Customers notified by
Two or more of the following: Email, Fax, Letter, Press Release, Telephone, Visit
Reason category
Salmonella
Product category
Other

Timeline

20 Jan 2018Recall initiated by company
15 Feb 2018Classified by FDA+26 days
21 Feb 2018Published in enforcement report+6 days

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

Reason for recall

Product may be contaminated with Salmonella.

Salmonella causes fever, diarrhea and abdominal cramps, usually 12 to 72 hours after eating contaminated food. Most people recover without treatment, but severe cases can need hospital care.

Product as listed by the FDA

Zero for Him 150 count

Where it was distributed

Direct to MA and PA

MassachusettsPennsylvania

Questions about this recall

Is Zero for Him recalled?

Yes. ABH Nature's Products recalled Zero for Him on 20 Jan 2018. The recall is Class I and its status is Terminated. Recall number F-0813-2018.

Why was it recalled?

Product may be contaminated with Salmonella.

Which lots are affected?

Lot#1710638B

Where was it sold?

Direct to MA and PA

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 I mean?

Class I is the most serious FDA recall category: there is a reasonable probability that using the product will cause serious health consequences or death.

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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