Klaire Labs is recalling children's probiotic supplements after blue glass shards were found in some bottles. This hazard poses a choking risk for young children. Consumers should check product lot numbers and contact the company for details.
Firm is recalling three lots of Ther-Biotic dietary supplements due to reports of shards of blue glass found in the bottles, not the in supplement.
Klaire Labs is recalling children's probiotic supplements due to blue glass shards found in some bottles. This could cause choking or injury to young children who might swallow the shards.
The supplements contain blue glass shards that can be swallowed by children. These shards could cause choking, lacerations, or internal injuries if ingested. The hazard is not present in all products but only in specific lots.
Parents and caregivers of children who use this probiotic supplement are most at risk. Children under 5 years old are particularly vulnerable due to their small size and tendency to put objects in their mouth.
Check the product label for the lot number J4694 and expiration date 12/15. The product is sold under the brand Klaire Labs Ther-Biotic Children's Chewable Probiotic.
Look for the lot number J4694 and expiration date 12/15 on the bottle.
No, the product contains blue glass shards that could cause injury if swallowed. Do not use this specific lot.
Check the product label for lot number J4694 and expiration date 12/15. This product is sold under Klaire Labs Ther-Biotic Children's Chewable Probiotic.
Check the product label for the lot number. If it matches J4694, contact Klaire Labs for instructions.
We’ve drafted a message you can send Kla:re Labs to request your refund or repair — edit it as you like.
Subject: Recall F-1954-2015 — Kla:re Labs Kla:re Labs Hello, I own a Kla:re Labs that is covered by recall F-1954-2015 from Kla:re Labs. I’m writing to arrange the remedy described in the recall (a refund, repair, or replacement as applicable). Could you please tell me the next steps to resolve this? Thank you.
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The facts (hazard, remedy, dates, manufacturer) are pulled from the official FDA recall record. The plain-language summary and step-by-step checklist are written by GovInfoNow to make the official notice easier to act on — they don’t replace it.
