Stage 2 World Baby
Reason Intermittent damage to the plastic spouts during manufacturing of two varieties of Plum products on two product dates may cause plastic fragments to break loose and cause a potential choking hazard.
Stage 2 World Baby Thailand recall
Recalled by Plum Inc · Emeryville, CA, United States
Class II — Moderate risk. May cause temporary or reversible harm; serious harm unlikely.
Why it was recalled
Intermittent damage to the plastic spouts during manufacturing of two varieties of Plum products on two production dates may cause plastic fragments to break loose and cause a potential choking hazard.
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
Stage 2 World Baby Thailand; Roasted Pumpkin & Coconut Rice, 3.5 oz. pouch. Product of USA distributed by Plum Inc., Emeryville, CA
Quantity: 11,595 total cases, both varieties. 12 x 3.5 oz pouches per case.
Food: Pasta, rice & grains
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.
Best Before 10SEP14
Where it was sold
FDA's distribution note: US and small quantities exported to Hong Kong, Singapore and Malaysia.
Check the codes, then return or discard. Class II means eating it may cause temporary or reversible health problems. If your package matches the recalled codes, do not eat it - return it to the store or throw it away. 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
- Plum Inc
- Initiated by
- Voluntary: Firm initiated
- Recall initiated
- Mar 4, 2014
- In FDA report of
- Apr 2, 2014
- Terminated
- Jul 17, 2015
- FDA recall number
- F-1687-2014 · event 67660
- 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.
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