C.R. Bard recalls BD Heyman Follower Coude Tips for sizes 12Fr, 14Fr, and 16Fr due to potential incorrect French size labeling in packaging. Affected units include specific lot and UDI numbers.
Cather packaging may contain the incorrect French size.
C.R. Bard is recalling BD Heyman Follower Coude Tips for sizes 12Fr, 14Fr, and 16Fr because the packaging might have the wrong French size. This could lead to incorrect use if the size is misread.
The packaging may contain the incorrect French size, which could result in using the wrong size during medical procedures. This might cause improper fit or function if the size is misread.
Users of BD Heyman Follower Coude Tips for medical procedures who purchased these specific sizes between the listed dates. Healthcare professionals and patients using the product are most at risk.
Check the product's reference number (REF) and lot number on the packaging. For 12Fr: REF:021312, Lot:JUJX0285; 14Fr: REF:021314, Lot:JUJX1147; 16Fr: REF:021316, Lots:JUJY0895 & JUJX1148.
Look for the reference number (REF) and lot number on the packaging to confirm if it matches the listed affected units.
The recall is due to potential incorrect French size labeling in the packaging, which could lead to using the wrong size during medical procedures.
Sizes 12Fr, 14Fr, and 16Fr with specific reference numbers and lot numbers listed in the recall notice.
Check the product's reference number (REF) and lot number on the packaging. Affected units include REF:021312 (Lot:JUJX0285), REF:021314 (Lot:JUJX1147), and REF:021316 (Lots:JUJY0895 & JUJX1148).
We’ve drafted a message you can send C.R. Bard to request your refund or repair — edit it as you like.
Subject: Recall Z-2075-2025 — C.R. Bard C.R. Bard Hello, I own a C.R. Bard that is covered by recall Z-2075-2025 from C.R. Bard. 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.
