DISP.TROCAR W.DILATING PIN 12/110MM, Product Code EK234SU. For use in laparoscopic procedures.
Reported: March 13, 2024 Initiated: January 9, 2024 #Z-1245-2024
Product Description
DISP.TROCAR W.DILATING PIN 12/110MM, Product Code EK234SU. For use in laparoscopic procedures.
Reason for Recall
The sterile blister packaging may be damaged, and sterility may be compromised.
Details
- Recalling Firm
- Aesculap Inc
- Units Affected
- 6 pieces
- Distribution
- Worldwide - US Nationwide distribution in the states of KS, NJ and NY. The country of Canada.
- Location
- Center Valley, PA
Frequently Asked Questions
What product was recalled? ▼
DISP.TROCAR W.DILATING PIN 12/110MM, Product Code EK234SU. For use in laparoscopic procedures.. Recalled by Aesculap Inc. Units affected: 6 pieces.
Why was this product recalled? ▼
The sterile blister packaging may be damaged, and sterility may be compromised.
Which agency issued this recall? ▼
This recall was issued by the FDA Devices on March 13, 2024. Severity: Moderate. Recall number: Z-1245-2024.
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