Severity
Moderate
FDA Food recall · Reported December 4, 2013
Food supplement products were made from ingredients that are contaminated with Chloramphenicol.
Pacific Nutritionals recalled -DigestMORE, 90 capsules per bottle, Food Supplement is sold under Renew Life brand. Th… - a moderate-severity action.
-DigestMORE, 90 capsules per bottle, Food Supplement is sold under Renew Life brand. Th… was recalled by Pacific Nutritionals in December 4, 2013. Reason: Food supplement products were made from ingredients that are contaminated with Chloramphenicol.. Check the official notice for the remedy. Verify recall #F-0347-2014 with the FDA Food before acting.
The recall
Pacific Nutritionals issued this moderate-severity FDA Food recall-Food supplement products were made from ingredients that are contaminated with Chloramphenicol..
Sourced from official FDA Food enforcement records. Verify recall #F-0347-2014 with the agency before acting. Full product description, hazard, remedy, and related recalls are below.
This FDA Food action (record #F-0347-2014) was formally reported on December 4, 2013, with the manufacturer initiating the action on October 1, 2013. It is classified under Moderate severity (Class II), with a current status of Terminated. Pacific Nutritionals is listed as the recalling firm, operating out of Vancouver, WA. Federal records list the affected scope as 1008 bottles of DigestMORE; 1008 bottles of DigestMORE Ultra.
The documented reason for this recall is: Food supplement products were made from ingredients that are contaminated with Chloramphenicol. Distribution data in the federal record shows the product reached: Distributed to Florida and Canada.. Distribution scope directly affects the consumer exposure window and determines whether a recall remains regional or escalates into a nationwide advisory.
Within the same product category the archive holds 6 closely related recalls, 2 from FDA Food - clustering in a narrow category often points to a systemic quality-control or supplier issue rather than a one-off defect. Always verify the recall number against the official agency record before acting.
Where this recall sits in its category - 25,126 food recalls on record
Of 101,704 recalls in the database, 24,878 are high severity, 72,426 moderate, and 4,400 low. This recall is classified moderate severity.
Counts reflect market size and reporting activity, not inherent danger, we do not rank products by risk from raw recall volume.
Severity
Moderate
Affected scope
1008 bottles of DigestMORE; 1008 bottles of DigestMORE Ultra
Related Recalls
6
2 from same agency
-DigestMORE, 90 capsules per bottle, Food Supplement is sold under Renew Life brand. The UPC Code 6 31257 35000 8. -DigestMORE Ultra, 60 capsules per bottle, Food Supplement is sold under Renew Life brand. The UPC Code 6 31257 35001 5. The DigestMORE product is labeled in parts: "***DigestMORE***RENEW LIFE***The Digestive Care Company***90 Capsules***Food Supplement***RENEW LIFE UK***Unit 3, 12 Commercial Road, Reading, Berkshire***RG2 0QJ***www.renewlife.co.uk***. The DigestMORE Ultra product is labeled in parts: "***DigestMORE Ultra***RENEW LIFE***The Digestive Care Company***60 Capsules***Food Supplement***RENEW LIFE UK***Unit 3, 12 Commercial Road, Reading, Berkshire***RG2 0QJ***www.renewlife.co.uk***.
Food supplement products were made from ingredients that are contaminated with Chloramphenicol.
| Attribute | Value |
|---|---|
| Agency | U.S. Food and Drug Administration |
| Severity class | Moderate (Class II) |
| Status | Terminated |
| Recall number | F-0347-2014 |
| Date reported | December 4, 2013 |
| Date initiated | October 1, 2013 |
| Recalling firm | Pacific Nutritionals |
| Firm location | Vancouver, WA |
| Affected scope | 1008 bottles of DigestMORE; 1008 bottles of DigestMORE Ultra |
| Distribution | Distributed to Florida and Canada. |
Profile values are sourced directly from the official FDA Food enforcement record. Source: U.S. Food and Drug Administration.
What to do with this recall
Match your product against the recall record, then act on the agency remedy.
This page summarizes the official FDA Food record for research and awareness; it is not legal, medical, or safety advice. Verify with the issuing agency before acting.
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Every figure on PlainRecalls is rendered directly from official FDA, CPSC and NHTSA recall records, no number is typed in by an editor. This recall: FDA Food, reported December 4, 2013. Severity classes follow each agency's own taxonomy (FDA Class I/II/III; CPSC and NHTSA by hazard type), and related-recall context is computed across the full archive. See our editorial standards & corrections policy, the methodology behind these numbers, or report a data error. Data current as of July 2026.