[pending] Product Name: MIC Safety Percutaneous Endoscopic Gastrostomy PEG Kit 14 Fr PUSH OTW Model/Catalog
Pending LLM rewrite. Source: FDA_DEVICE Z-2341-2026.
What this means for you
Real risk of harm even if no illness or injury has been reported yet. Stop using the product and follow the agency's guidance.
Our severity reasoning: Pending LLM scoring against the rubric.
Plain-English summary
Lidocaine hydrochloride injection, the subject of a supplier recall for quality issues, were included into sterile kits and sets.
The recalled product
- Product
- Product Name: MIC Safety Percutaneous Endoscopic Gastrostomy PEG Kit 14 Fr PUSH OTW Model/Catalog Number: 7170-14 Product Description: Feeding Tube Kit
- Manufacturer
- Avanos Medical, Inc.
- Category
- Medical Device — Devices
Is your product affected?
Check your packaging against the codes below. If any of them match, the product is part of this recall.
Lot numbers (2)
- UDI-DI 10350770007752
- Lot Number 30370713
Distribution
Distributed nationwide across the United States.
Related recalls
Same category
- SevereTMINI Tracking Array knob loosening causing potential array misalignment
FDA (Devices) · 2026-07-15
- ModerateVersius Surgical System Console affected by cybersecurity vulnerability
FDA (Devices) · 2026-07-15
- Moderate5008X Blood Tubing Set connection errors FDA Class II recall
FDA (Devices) · 2026-07-15
- ModerateMedline Convenience Kits containing temperature probes recalled
FDA (Devices) · 2026-07-15
- SevereFletcher CT/MR Shielded Applicator Set for Gynecological Brachytherapy Recalled
FDA (Devices) · 2026-07-15