Reported Jul 10, 2024 · Completed
AMT Initial Placement Dilator Set. Used to place gastrostomy devices.
Applied Medical Technology Inc.
Moderate riskThis product could cause temporary or reversible health problems — stop using it.What you should do
Stop using the affected lot and contact the recalling firm for the return or refund process. Check the FDA enforcement report for lot-level detail.
Firm contact: Applied Medical Technology Inc · 8006 Katherine Blvd · Brecksville, OH · 44141-4202
Is this the product you have?
- AMT Initial Placement Dilator Set. Used to place gastrostomy devices.
- Lot codes and dates
- Model NoIP-DIL
- UDI-DI00842071131876
- Lot number231218-242; Exp
- Date2026-11-01
- Amount recalled
- 74 units
Where it was sold
Why it was recalled
Devices were labelled with the incorrect guidewire labelling.
This product could cause temporary or reversible health problems — stop using it.
Want the full recall guide?
The guide adds the identifying codes laid out for scanning, symptoms to watch for, a timeline, and news coverage of this recall.
Free recall alerts
Get alerted about new Applied Medical Technology Inc. recalls
One email when a matching recall is published. No account, no cost, unsubscribe in one click.
We email you about recalls and nothing else. Every send has a one-click unsubscribe, and you can change your preferences any time without an account.