H:20 Innovations recalls Meijer Baby Pediatric Electrolyte Strawberry Flavor 8oz drinks with seal defect found in complaint investigation. Products sold with Best by 10/02/15.
H:20 Innovations is recalling Meijer Brand Baby Pediatric Electrolyte Fruit and Strawberry Flavor 8oz drinks due to a seal defect found during a complaint investigation.
H:20 Innovations is recalling Meijer Baby Pediatric Electrolyte Strawberry Flavor 8oz drinks because of a seal defect. This defect could lead to contamination or leakage, making the product unsafe for infants.
The seal defect may allow contaminants to enter the product or cause leakage, potentially leading to contamination or spills. This poses a risk of infant illness or injury if the product is not properly sealed.
Parents or caregivers of infants who purchased Meijer Baby Pediatric Electrolyte Strawberry Flavor 8oz drinks with Best by date 10/02/15 are most at risk.
Check for the product name 'Meijer Baby Pediatric Electrolyte Strawberry Flavor 8oz x 4', Best by date 10/02/15, and lot number P0127513 on the packaging.
Look for the Best by date 10/02/15 and lot number P0127513 on the packaging.
The product has a seal defect and is recalled, so it is not safe for use. H:20 Innovations is recalling it due to potential contamination risks.
Check for the product name 'Meijer Baby Pediatric Electrolyte Strawberry Flavor 8oz x 4', Best by date 10/02/15, and lot number P0127513 on the packaging.
The recall record does not specify a remedy, so contact H:20 Innovations for guidance on next steps.
We’ve drafted a message you can send H:20 Innovations to request your refund or repair — edit it as you like.
Subject: Recall F-1953-2014 — H:20 Innovations H:20 Innovations Hello, I own a H:20 Innovations that is covered by recall F-1953-2014 from H:20 Innovations. 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.
