Medical Device
Manufacturing
THE TRADE PAPER OF THE FACTORY FLOOR
Z-1475-2025Class II

Otopore Square outer ear wound dressing, Firm Catalog Number 5400-020-100 and Forte Catalog Number...

Stryker Corp. / initiated 2025-02-25 / Open, Classified / root cause: packaging

Stryker Corporation began a recall of Otopore Square outer ear wound dressing, Firm Catalog Number 5400-020-100 and Forte Catalog Number 5400-020-100ITL on . FDA classified it as Class II and gives the reason as "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". As of , the recall status on record is Open, Classified, and MDM tags the root cause as packaging.

Recall record

Recall number
Z-1475-2025
Classification
Class II
Status
Open, Classified
Initiated
Posted
Recalling firm
Stryker Corp.
Product
Otopore Square outer ear wound dressing, Firm Catalog Number 5400-020-100 and Forte Catalog Number 5400-020-100ITL
Product code
NHB Polymer, Ear, Nose And Throat, Synthetic, Absorbable
Reason for recall
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.
Root cause tag
packaging
FDA root cause
Under Investigation by firm
Action
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.
Quantity in commerce
182,344 total units
Distribution
US Nationwide distribution.
Product codes and lots
5400-020-100 UDI-DI: 07613327301656, Lot Numbers: 2022101016 2023021716 2023062115 2023082113 2024022114; 5400-020-100ITL UDI-DI: 07613327359497, Lot Numbers: 2023021715 2023100214 2023102315 2024012414 2024022615 2024041015 2024052114 2024082713 2023072513 2023100515 2023102615 2024012914 2024030515 2024041714 2024052415 2023082114 2023101015 2023111515 2024020117 2024030815 2024042214 2024060412 2023082915 2023101312 2024010813 2024021315 2024031314 2024050713 2024072912 2023092532 2023101815 2024011115 2024021615 2024040515 2024051414 2024081415

Enforcement reports

One row per recalled product line
FDA enforcement reports joined to recall event Z-1475-2025
Recall numberClassStatusVoluntary or mandatedReport dateClassified
Z-1469-2025Class IIOngoingVoluntary: Firm initiated
Z-1470-2025Class IIOngoingVoluntary: Firm initiated
Z-1471-2025Class IIOngoingVoluntary: Firm initiated
Z-1472-2025Class IIOngoingVoluntary: Firm initiated
Z-1473-2025Class IIOngoingVoluntary: Firm initiated
Z-1474-2025Class IIOngoingVoluntary: Firm initiated
Z-1475-2025Class IIOngoingVoluntary: Firm initiated
Z-1476-2025Class IIOngoingVoluntary: Firm initiated
Z-1477-2025Class IIOngoingVoluntary: Firm initiated
Z-1478-2025Class IIOngoingVoluntary: Firm initiated
Z-1479-2025Class IIOngoingVoluntary: Firm initiated
Z-1480-2025Class IIOngoingVoluntary: Firm initiated
Z-1481-2025Class IIOngoingVoluntary: Firm initiated
Z-1482-2025Class IIOngoingVoluntary: Firm initiated