How to Check if Your Medical Device Has Been Recalled

Last reviewed Oct 16, 2026 · Based on FDA sources listed below · Editorial policy

Medical device recalls rarely cover every unit of a product. Most apply to specific models, lot numbers or software versions — so the real question is not "was this product recalled?" but "is my device affected?".

Step 1: Find your device's identifiers

Look on the device label, the box, or the instructions that came with it. You are looking for:

Brand and model name (for example "Dexcom G7 Receiver").
Model, catalog or REF number.
Lot or serial number — often next to a "LOT" or "SN" symbol.
UDI — the number printed under the barcode. The part after "(01)", usually 14 digits, is the device identifier and points to the exact model.

For implants, ask your surgeon's office or the hospital for your implant record card; it lists the model and lot.

Step 2: Search the recall records

Search your device on this site. Each device page lists the FDA recall records that name its identifier, and each product page — for example Omnipod 5 — groups all models of a product.
The FDA's own Medical Device Recalls database is the official source.
The manufacturer's website often has a recall lookup where you type your lot or serial number.

Step 3: Compare the code information

Every recall record has a "code information" section listing the affected models, lots or serial numbers. If your numbers appear there, your device is affected. If it says "all lots" or "all serial numbers", every unit of that model is included.

Step 4: If your device is affected

Follow the instructions in the recall notice and from the manufacturer. Some recalls mean returning the device; others mean a software update, a new label or extra checks.
Do not stop using a prescribed or implanted device on your own. Call your healthcare provider: for many recalls the safest step is to keep using the device with extra precautions until a fix or replacement is arranged.
If you rely on the device every day, keep a backup plan (for example insulin pens if your pump is affected).

Step 5: Stay informed

Register your device with the manufacturer if it offers registration — that is how many companies contact affected users directly. You can also come back to your device's page here; it is rebuilt when the FDA publishes new data.

This guide explains public FDA information. It is not medical advice — talk to your healthcare provider about decisions involving your device.