Multi for Him (Full Strength Mini and Multi Softgels), 60 Count Bottle
What you need to know
Class II
What happened
Pharmavite LLC is conducting a voluntary recall of all lots of its Nature Made Full Strength Mini Multivitamins (recently repackaged as "Multi" softgels, (Multi Complete, Multi…
Health risk
The product may cause temporary or medically reversible health consequences, or the probability of serious harm is remote. A safety issue that does not fit the standard pathogen, allergen, chemical or quality categories.
Action required
Stop taking the supplement. Check the lot and UPC codes below, then return it to the retailer or contact the manufacturer about a refund. Seek medical advice if you have concerns about exposure.
Recall closed · classified by the FDANationwide (US)More supplements
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Pharmavite CorporationNorthridge, CA, United States
UPC / barcodes
28 640316 04028 60 31604 02864 0
Lot / date codes
All lots. UPC Code 2864 0-31604-02864-0. List # 2864.
Distribution area
Nationwide
US nationwide. No International.
United States
Quantity affected
130, 280 bottles
Recall initiation
FDA report date: November 27, 2013
FDA recall number
F-0187-2014
Beyond the headline
The recall, in context
Pharmavite Corporation initiated this supplements recall on September 9, 2013. The FDA enforcement report states: Pharmavite LLC is conducting a voluntary recall of all lots of its Nature Made Full Strength Mini Multivitamins (recently repackaged as "Multi" softgels, (Multi Complete, Multi for Her, Multi for Her 50+, Multi for Him, Multi Complete club size). because recent quality tests indicate that the Vitamins B1 and B12 are losing potency more rapidly than initially expected, and these products are not me. The FDA report lists distribution as: US nationwide. No International.
The FDA enforcement report describes the reason as: Pharmavite LLC is conducting a voluntary recall of all lots of its Nature Made Full Strength Mini Multivitamins (recently repackaged as "Multi" softgels, (Multi Complete, Multi for Her, Multi for Her 50+, Multi for Him, Multi Complete club size). because recent quality tests indicate that the Vitamins B1 and B12 are losing potency more rapidly than initially expected, and these products are not me
Multi for Him (Full Strength Mini and Multi Softgels), 60 Count Bottle was made or distributed by Pharmavite Corporation in Northridge, CA, United States. This page reflects FDA report F-0187-2014, dated November 27, 2013.
Why this is a Class II recall
Class II means the product may cause temporary or medically reversible health consequences, or the probability of serious harm is remote. In this recall, a safety issue that does not fit the standard pathogen, allergen, chemical or quality categories.
FDA definition
The product may cause temporary or medically reversible health consequences, or the probability of serious harm is remote.
What to do now
1
Stop using it
Do not eat, drink or take the affected product.
2
Check the codes
Compare the UPC and lot code against the table above.
3
Return or discard
Contact the retailer or recalling firm about a refund, and dispose of the product safely.
Consumer safety guide
Product safety recall
Symptoms to watch for
The official enforcement report describes the specific risk. Follow the recall notice, check the product codes and do not use a product that may be affected.
Higher-risk groups
Children, pregnant people, older adults and people with weakened immune systems should take extra care when a product's safety is uncertain.
What to do now
1Stop using or eating the product and keep it away from children and pets.
2Check the UPC and lot/date codes on this page and follow the official recall notice for disposal or return.
3Seek medical advice if anyone develops severe or worrying symptoms after exposure.
Read the official source record for the specific hazard and instructions.
This is general consumer safety information, not medical advice or a diagnosis. Follow the official recall notice and contact a healthcare professional if you have concerns about exposure or symptoms.
Frequently asked
Questions about this recall
7 answers
What is the Multi for Him (Full Strength Mini and Multi Softgels), 60 Count Bottle recall?
Pharmavite Corporation recalled Multi for Him (Full Strength Mini and Multi Softgels), 60 Count Bottle in an FDA Class II enforcement action reported as F-0187-2014. Pharmavite LLC is conducting a voluntary recall of all lots of its Nature Made Full Strength Mini Multivitamins (recently repackaged as "Multi" softgels, (Multi Complete, Multi…
What are the symptoms of Product safety recall exposure?
The official enforcement report describes the specific risk. Follow the recall notice, check the product codes and do not use a product that may be affected.
Who is most at risk from Product safety recall?
Children, pregnant people, older adults and people with weakened immune systems should take extra care when a product's safety is uncertain.
What should I do if I bought this product?
Stop taking the supplement. Check the lot and UPC codes below, then return it to the retailer or contact the manufacturer about a refund. Seek medical advice if you have concerns about exposure. Stop using or eating the product and keep it away from children and pets. Check the UPC and lot/date codes on this page and follow the official recall notice for disposal or return. Seek medical advice if anyone develops severe or worrying symptoms after exposure.
How do I get a refund from Pharmavite Corporation?
Contact the recalling company or the retailer where you purchased the product, quote the FDA recall number and ask about a refund or replacement. Keep the packaging, lot code and proof of purchase where possible. The FDA does not issue consumer refunds. Reference FDA recall F-0187-2014 and keep the packaging, lot code and proof of purchase if you have them.
Is the Pharmavite Corporation recall still active?
The FDA lists this recall as recall closed. It remains relevant if you still have the affected product or need to identify a historical recall.
Where can I verify this recall?
This page is normalized from the openFDA enforcement record F-0187-2014. You can verify it directly using the official source link on this page. VerifyRecall updates its index from public FDA enforcement data and does not replace advice from the FDA, the recalling firm or a healthcare professional.
Verify before you act.
VerifyRecall is independent and not affiliated with the FDA. Always confirm the latest status on the official source record.