CLASS II Food recall · Reported 5 Feb 2014 · FDA Enforcement Report

Digest Ultra, dietary supplement, packaged per bottle recalled

Health Wright Products is recalling Digest Ultra, dietary supplement, packaged per bottle, distributed in California, Florida, Oregon, Utah. The recall was initiated on 25 Oct 2013 and the FDA has classified it as Class II.

Check your package

Lot, batch or date codesLOT Numbers: 1207408; MFG -03/12; 1217703; MFG -06/12; 10190112; MFG -01/12; 10190112; MFG -01/12; 10190312; MFG-03/12; 10190313; MFG -03/13; 10191112; MFG -11/12; 20190313; EXP- 2/2015; 20190612; EXP- 06/14; 20191012; EXP -10/14; 1019A0811; EXP- 08/13 ;
Quantity recalled82,906 bottles and 1,552,319 capsules (bulk) in US and 62766 bottles OUTSIDE the US

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-1461-2014
FDA event ID
66843
Recalling firm
Health Wright Products, Clackamas, OR
Classification
Class II
Status
Terminated
Recall initiated
25 Oct 2013
FDA classified
30 Jan 2014
Reported
5 Feb 2014
Type
Voluntary: Firm initiated
Customers notified by
Two or more of the following: Email, Fax, Letter, Press Release, Telephone, Visit
Reason category
Packaging Defects
Product category
Dietary Supplements

Timeline

25 Oct 2013Recall initiated by company
30 Jan 2014Classified by FDA+97 days
5 Feb 2014Published 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

Dietary supplement products are recalled because they were made from ingredient that was contaminated with Chloramphenicol.

Packaging recalls include wrong labels, wrong products in the wrong bottle, missing leaflets, short-filled or empty capsules and seals that fail.

Product as listed by the FDA

Digest Ultra, dietary supplement, packaged 56 capsules per bottle or distributed in bulk, sold under brand YOR. Product distributed OUTSIDE the US has Spanish label.

Where it was distributed

Distributed to California, Florida, Oregon, Utah, and Mexico

CaliforniaFloridaOregonUtah

Questions about this recall

Why was it recalled?

Dietary supplement products are recalled because they were made from ingredient that was contaminated with Chloramphenicol.

Which lots are affected?

LOT Numbers: 1207408; MFG -03/12; 1217703; MFG -06/12; 10190112; MFG -01/12; 10190112; MFG -01/12; 10190312; MFG-03/12; 10190313; MFG -03/13; 10191112; MFG -11/12; 20190313; EXP- 2/2015; 20190612; EXP- 06/14; 20191012; EXP -10/14; 1019A0811; EXP- 08/13 ;

Where was it sold?

Distributed to California, Florida, Oregon, Utah, and Mexico

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 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

8 other products · FDA event 66843

This product is part of a recall event; the main page for the event is Zinc Plus, Mineral/Enzyme supplement recalled by Health Wright Products.

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