Shot glasses with decorative artwork that reads Blue
Reason Through internal compliance and independent laboratory product testing program, the company became aware that glassware exceeded the FDA's guidance levels for lead and cadmium.
Pint sized glasses with decorative artwork that reads Blue recall
Recalled by Charles Products Inc · Rockville, MD, United States
Class I — High risk. Reasonable probability of serious harm or death.
Why it was recalled
Through internal compliance and independent laboratory product testing program, the company became aware that glassware exceeded the FDA's guidance levels for lead and cadmium.
Hard or sharp fragments can cut the mouth or throat, break teeth or cause choking. They usually come from equipment wear or packaging on the production line. All foreign material recalls.
What was recalled
Pint sized glasses with decorative artwork that reads Blue: "Who's Your Candy?!" SKU # 835992 Green: "Eye Candy" SKU # 835993 Red: "Hard on the Outside Sweet on the Inside" SKU # 835991
Quantity: 8,640
Lot codes, dates and UPCs
A recall covers only these codes. Compare them with the lot number, best-by date or UPC printed on your package.
Blue pint glasses: material #2000835992 Green pint glasses: material #2000835993 Red pint glasses: material #2000835991
Where it was sold
Florida Nevada New York
FDA's distribution note: Available exclusively through M&M's World Retail Stores in New York, NY; Orlando, FL; Las Vegas, NV; and London, UK.
Do not eat it. Class I means FDA judged there is a reasonable probability of serious illness or death. If the brand, size and lot or date code on your package match, throw the product away or return it to the store for a refund, and clean any surface or container it touched. If anyone has eaten it and feels unwell, contact a doctor and mention the recall. FDA lists this recall as terminated: the company has finished removing the product, so it should no longer be on shelves - but it can still be in a freezer or pantry.
- Recalling firm
- Charles Products Inc
- Initiated by
- Voluntary: Firm initiated
- Recall initiated
- Apr 18, 2014
- In FDA report of
- Aug 12, 2015
- Terminated
- Aug 6, 2015
- FDA recall number
- F-2929-2015 · event 68340
- Official record
- FDA enforcement report search
Also recalled with it (1 more product)
FDA files each product of one recall action separately; these share the same FDA event.