Dial-A-Dose Insulin Delivery Device recall
Dial-A-Dose Insulin Delivery Device (Pen-Injector) cartridge holders Product Usage: The NovoPen Echo¿ is a re-usable pen injector for single patient…
Why was Dial-A-Dose Insulin Delivery Device recalled?
A small number of batches may crack or break if exposed to certain chemicals, like certain cleaning agents.
What should I do if I have this product?
Review the official FDA enforcement record for current instructions.
What to do with a recalled product: refunds, receipts, safe disposal and how to report a problem.
Is my product affected?
Compare the item in your hand with every identifier below from the official FDA record. Only products that match the listed product and lot, UPC or model codes are part of this recall.
Which lot codes, UPCs or models are affected?
U.S. batch numbers: EVG1221, EVG1226, FVG7149, FVG7458, FVG8134 & FVG8135
- Product
- Dial-A-Dose Insulin Delivery Device (Pen-Injector) cartridge holders Product Usage: The NovoPen Echo¿ is a re-usable pen injector for single patient…
- Recalling firm
- Novo Nordisk Inc
- Quantity
- 16,557 units
- Distribution
- Nationwide distribution
- Recall date
- December 13, 2017
- Classification
- Class II
- Status
- Terminated
- Agency
- FDA (device)