FDA Food Recalls

Recalls / Class II

Class IIF-0838-2014

Product

Nature's Way,UPC 33674156865, Alive Once Daily Women's Ultra Potency, 60 Tabs, 20010554, 20011595, 20014135

Type
Food
Affected lot / code info
20010554, 20011595, 20014135
Quantity
23156

Why it was recalled

Nature's Way (NW) is voluntary recalling a number of products because the raw material supplier informed them that enzymes in the blend they provided to NW may contain the antibiotic chloramphenicol.

Recalling firm

Firm
Schwabe North America, Inc.
Notification channel
Letter
Type
Voluntary: Firm initiated
Address
825 Challenger DR, N/A, Green Bay, Wisconsin 54311-8328

Distribution

Distribution pattern
US: AK, AL, AR, AZ, CA, CI, CT, DC, FL, GA, HI, IA, ID, IL, IN, KS, KY, LA, MA, MD, ME, MI, MN, MO, NS, NT, NC, ND, NE, NH, NJ, NM, NV, NY, H, OK, OR, PA, PR, RI,SC, SD, TN, TX, UT, VA, VT, WA, WI, WV, WY. OUS: South Korea, Ghana, Romania and Singapore.

Timeline

Recall initiated
2013-10-23
FDA classified
2013-12-16
Posted by FDA
2013-12-25
Terminated
2015-02-26
Status
Terminated

Source: openFDA Food Enforcement endpoint. Recall record F-0838-2014. The FDA issues recall classifications as health-hazard assessments, not legal findings.

Class II food recall: Nature's Way,UPC 33674156865, Alive Once Daily Women's Ultra Potency, 60 Tabs, 20010554, 20011595,… · FDA Food Recalls