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Hemopore recallZ-1482-2025 · Stryker Corporation · initiated Feb 25, 2025

Open, Classified

Is my device affected?

  1. Compare the model, catalog and lot or serial numbers on your device or its packaging with the code information below. A recall usually covers only specific models or lots.
  2. If yours is listed, follow the instructions from Stryker Corporation or your healthcare provider. The company's action is summarized under what the company is doing.
  3. Do not stop using a prescribed or implanted device on your own — talk to your healthcare provider first.

Where to find your model and lot numbers · What recall classes and statuses mean

Why it was recalled

There is a potential for blister seals on the product to present a bubble on the seal area of the packaging. This seal acts as a sterile barrier and, in this event, indicates that the sterility seal has been breached.

FDA root cause category: Under Investigation by firm

What the company is doing

An Urgent Medical Device Recall notification letter dated 2/24/25 was sent to customers. Actions to be taken 1. Immediately review your inventory to locate and quarantine any affected products at your facility. 2. Return the enclosed Business Reply Form (BRF), even if the affected product is no longer in inventory, to the email [email protected]. 3. Upon receipt of the completed BRF, Stryker will provide a shipping label to return recalled product on-hand. 4. A replacement will be provided upon receipt of the recalled product. 5. Maintain awareness of this communication internally and inform Stryker if any of the subject devices have been distributed to other organizations. If so, provide contact details so Stryker can inform the recipients accordingly. [email protected]. RESPONSE IS REQUIRED.

Recall details

Recall number
Z-1482-2025
Status
Open, Classified
Initiated by the company
Feb 25, 2025
Posted by the FDA
Mar 28, 2025
Recalling firm
Stryker Corporation
Quantity
182,344 total units
Product code
NHB
FDA submissions
K070715
Distribution
US Nationwide distribution.

Product description

Hemopore 2PK nasal/sinus temporary wound dressing, Catalog Number 5400-222-208S

Code information (models, lots, serial numbers)

5400-222-208S UDI-DI: 07613327500486, Lot Numbers: 2024020221 2024051720 2024082321

Devices named in this recall

1 device in the FDA device registry whose identifier appears in the recall's code information.

Product lines

Other products in the same recall event

The FDA groups related products into one recall event (event 96393).

Sources and updates

How recalls are matched to devices · Editorial policy · Report an error on this page