NOW Ginseng & Royal Jelly 90 VCAPS UPC 733739040077 MMA Nutrition Ginselin 90 Veg Capsules UPC 733739440075
Summary
The FDA issued a Class III for NOW Ginseng & Royal Jelly 90 VCAPS UPC 733739040077 MMA Nutrition Ginselin 90 Ve by NOW Health Group Inc.. Reason: Product may contain Metronidazole.
Details
Source
Food Recall
External ID
F-0156-2022
Action Date
2021-11-17
Status
Terminated
Category
food
Product Description
NOW Ginseng & Royal Jelly 90 VCAPS UPC 733739040077 MMA Nutrition Ginselin 90 Veg Capsules UPC 733739440075
Lot/Code Info: Lots: 3168920 3217381 3219743 (MMA Nutrition)
Quantity Affected: 7,935 units
Reason for Recall
Product may contain Metronidazole
Distribution
Total number of domestic consignees = 1576 (including 2 private label customers). Domestic online and retail to AK, AL, AR, AZ, CA, CO, CT, DE, FL, GA, IA, ID, IL, IN, KS, KY, LA, MA, MD, ME, MI, MN, MO, MS, MT, NC, ND, NE, NH, NJ, NM, NV, NY, OH, OK, OR, PA, SC, SD, TN, TX, UT, VA, VT, WA, WI, WY. Total number of foreign consignees = 21 (including 1 private label customer). International distribution to retail locations in Bulgaria, Cameroon, Canada, England, Germany, Holland, Kazakhstan, Netherlands, Nigeria, Poland, Singapore, Slovakia, Sweden, Ukraine, and United Arab Emirates. International distribution to a distributor in Cairo, Egypt.
Type: Voluntary: Firm initiated
Recall Initiated: 2021-10-01
Company
Bloomingdale, IL
Context & Analysis
This is a Class III recall. Class III recalls involve products unlikely to cause adverse health consequences, but that violate FDA regulations.
This was one of 82 food recalls issued in the same week, part of 204 food-related FDA actions this month.
NOW Health Group Inc. has 4 FDA actions in our database, including 4 recalls.
Frequently Asked Questions
What is a Class III recall?
A Class III recall involves products that are unlikely to cause adverse health effects but violate FDA labeling or manufacturing regulations.
What should I do if I have this product?
Stop using the product. Check the product against the specific lot numbers or identifiers listed in the recall. Contact the manufacturer (NOW Health Group Inc.) or your retailer for a refund or replacement. If you experienced adverse effects, report them to the FDA via MedWatch.
How often does NOW Health Group Inc. have FDA actions?
NOW Health Group Inc. has 4 FDA actions in our database, including 4 recalls and 0 device clearances.
Where can I find the official FDA record?
The official record is available on FDA.gov. Search for "F-0156-2022" on FDA.gov for the full record. You can also use the openFDA API to query this record programmatically.
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