Suntech Medical recalls 20-pack of neonate #4 blood pressure cuffs that contain incorrect #3 size cuffs. The mislabeling may lead to improper use during infant blood pressure measurements.
Product is mislabeled. The label on the package is for a size #4 cuff, but the incorrect size #3 cuff was placed in the package.
Suntech Medical is recalling a box of 20 neonate #4 blood pressure cuffs because they contain the wrong size (#3 instead of #4) for infants. Using these cuffs could lead to inaccurate blood pressure readings in newborns.
The product is mislabeled with the wrong size cuff (#3 instead of #:4) inside the package. This could cause inaccurate blood pressure readings in newborns, potentially leading to incorrect medical decisions.
Newborns and healthcare providers who use these cuffs for blood pressure measurements. Infants at risk of inaccurate readings due to the incorrect cuff size.
Check for the product name 'Suntech Medical Disposable, Neonate #4, 1-Tube, Male Bayonet, Blood Pressure Cuffs, Box of 20' on the package. The lot number is A4H201 and catalog number is 98-0400-98.
Verify the cuff size on the package matches the label (should be #4 for neonates).
The product is mislabeled with the wrong size cuff (#3 instead of #4) inside the package.
Check for the product name 'Suntech Medical Disposable, Neonate #4, 1-Tube, Male Bayonet, Blood Pressure Cuffs, Box of 20' on the package. The lot number is A4H201 and catalog number is 98-0400-98.
The recall record does not specify a remedy, so check the cuff size and contact Suntech Medical for further guidance.
We’ve drafted a message you can send Suntech Medical to request your refund or repair — edit it as you like.
Subject: Recall Z-2277-2019 — Suntech Medical Suntech Medical Hello, I own a Suntech Medical that is covered by recall Z-2277-2019 from Suntech Medical. 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.
