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FDA recall record

Dietary Supplement packaged in the following configurations: (1) 5357 NWC UltraEnzSup 90' packaged in 90 count capsule unlabeled bottles (SKU 50027); (2) 5357 NWC UltraEnzSup...

Recall F-0746-2014Class IITerminatedOctober 30, 2013

FDA classification. FDA Class I, II, and III are not the same as USDA FSIS classifications and are not a cross-agency safety score.

FDA listed a termination date of March 3, 2015. openFDA does not treat this as a live recall-status tracker.

Product described in an FDA recall

Dietary Supplement packaged in the following configurations: (1) 5357 NWC UltraEnzSup 90' packaged in 90 count capsule unlabeled bottles (SKU 50027); (2) 5357 NWC UltraEnzSup UNL 200 packaged in 200 count capsule unlabeled bottles (SKU 50028); (3) NWC Naturals Ultra Enzyme Support packaged in 200-(SKU 52466) and 90-(SKU 52467) count capsule bottles.

Manufactured exclusively for Natural Wellness Centers of America, Laguna Hills, CA.

Reason

Firm is recalling dietary supplements containing a raw material which may contain >0.3 ppb chloramphenicol

Products involved

Product descriptions are copied from the FDA recall record. They are not a current catalog and are not automatically matched to WhoMadeMyFood product pages.

  • Dietary Supplement packaged in the following configurations: (1) 5357 NWC UltraEnzSup 90' packaged in 90 count capsule unlabeled bottles (SKU 50027); (2) 5357 NWC UltraEnzSup UNL 200 packaged in 200 count capsule unlabeled bottles (SKU 50028); (3) NWC Naturals Ultra Enzyme Support packaged in 200-(SKU 52466) and 90-(SKU 52467) count capsule bottles.

    Manufactured exclusively for Natural Wellness Centers of America, Laguna Hills, CA.

Code information listed by FDA

Lot #'s: 50027001, 50028001, 52466045, 52466046, 52466047, 52466048, 52466049, 52466050, 52466052, 52467041, 52467042, 52467043, 52467044, and 52467046

Distribution and firm information

Recalling firm listed by FDA: National Enzyme Co

Firm location listed by FDA: Forsyth, MO, United States

Distribution reported by FDA: Domestic distribution of the product is nationwide with direct accounts in 27 states in all geographical regions. Foreign distribution consists of direct accounts in the following countries: Canada, China, Malaysia, Norway, Slovakia, South Korea, Sweden, Taiwan, and the United Kingdom.

Product quantity listed by FDA: 4,438 bottles

Source

Source: U.S. Food and Drug Administration (FDA), openFDA food enforcement reports.

Official FDA openFDA food enforcement record

Identifying an FDA recall record does not imply FDA endorsement of WhoMadeMyFood. Methodology.