Resect. Intest. Laparo-LF, Model DYNJ42667A - Product Usage: This is a type of convenience kit used in various surgeries including cardiac, abdominal, and neck surgeries.
Reported: January 13, 2021 Initiated: November 13, 2020 #Z-0779-2021
Product Description
Resect. Intest. Laparo-LF, Model DYNJ42667A - Product Usage: This is a type of convenience kit used in various surgeries including cardiac, abdominal, and neck surgeries.
Reason for Recall
The cylindrical sponge component is not x-ray detectable.
Details
- Recalling Firm
- Medline Industries Inc
- Units Affected
- 88
- Distribution
- Foreign distribution only - Canada.
- Location
- Northfield, IL
Frequently Asked Questions
What product was recalled? ▼
Resect. Intest. Laparo-LF, Model DYNJ42667A - Product Usage: This is a type of convenience kit used in various surgeries including cardiac, abdominal, and neck surgeries.. Recalled by Medline Industries Inc. Units affected: 88.
Why was this product recalled? ▼
The cylindrical sponge component is not x-ray detectable.
Which agency issued this recall? ▼
This recall was issued by the FDA Devices on January 13, 2021. Severity: Moderate. Recall number: Z-0779-2021.
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