Express Dry Seal Chest Drain recall in Canada: Sterility issue
In plain language
This recall involves the Express Dry Seal Chest Drain sold in Canada. It's being recalled because the water in the pre-packaged syringe may not be sterile. Stop using the product and follow the return/repair steps in the official notice.
What to do
- Stop using the product immediately.
- Check model/serial numbers if provided.
- Return, repair, or dispose of it as instructed.
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Affected products
Express Dry Seal Chest Drain
Model: 4000-100N
Lot: 469918, 467195, 472581, 474950, 469920, 469403, 471069
Why this matters
Sterility issue
Do I have this product?
This recall only applies to specific products. Follow the steps below to check.
- 1
Check the product name
Make sure your product name matches one of the affected products listed above.
- 2
Check the lot number
Lot numbers identify specific production batches.
Affected lots: 469918, 467195, 472581, 474950, 469920, 469403, 471069
- 3
Check the model number
Model numbers are typically on the product label or packaging.
Affected models: 4000-100N
If your product matches one or more of the details above, it may be affected by this recall.
If your product does not match these details, it is not affected by this recall.
When in doubt, always check the official notice.
Frequently Asked Questions
Why was this product recalled?
Sterility issue
What should consumers do?
Stop using the product immediately. Check model/serial numbers if provided. Return, repair, or dispose of it as instructed.
Where was the product sold?
This product was sold in Canada. For specific retailers or distribution areas, please check the official recall notice linked on this page.
Is there a health risk?
Yes, there may be a health risk. Sterility issue
When was this product recalled?
This product was recalled on January 5, 2024.
Is the ATRIUM MEDICAL CORPORATION brand affected by this recall?
Yes, ATRIUM MEDICAL CORPORATION products are affected by this recall. This recall involves the Express Dry Seal Chest Drain sold in Canada. It's being recalled because the water in the pre-packaged syringe may not be sterile. Stop using the product and follow the return/repair steps in the official notice.