Potential health hazard — use of or exposure to this product may cause temporary or medically reversible adverse health consequences.
Kimberly-Clark MIC PEG Kit - Pull Type The Kimberly-Clark MIC Recalled by Kimberly-Clark Corporation Due to The placement guidewire diameter is too large and...
What You Should Do
Stop using this product immediately. Do not consume, use, or distribute it.
Return the product to the place of purchase for a full refund. If you have questions, contact Kimberly-Clark Corporation directly.
Affected Products
Kimberly-Clark MIC PEG Kit - Pull Type The Kimberly-Clark MIC PEG Kits - Pull type are Percutaneous Endoscopic gastrostomy (PEG) tubes intended for a non-surgical "pull" endoscopic placement technique. The PEG tube is held in place during use with an external retention disk.
Quantity: 766 units
Why Was This Recalled?
The placement guidewire diameter is too large and does not pass-through the introducer needle during the placement procedure of the PEG Feeding Tube.
Where Was This Sold?
This product was distributed nationwide across all 50 states.
About Kimberly-Clark Corporation
Kimberly-Clark Corporation has 19 total recalls tracked by RecallDetector.
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Data sourced from the FDA (Device). Last updated March 26, 2026. View original report