MEDLINE KIT CV I II, REF DYNJ906071B
Reported: October 23, 2024 Initiated: August 28, 2024 #Z-0123-2025
Product Description
MEDLINE KIT CV I II, REF DYNJ906071B
Reason for Recall
Medline Industries, LP. has identified certain kits containing the recalled Medtronic lots of the DLP Vessel Cannulae. During manufacturing of the three listed lot numbers, product for model 30001 was incorrectly labeled as model 30000.
Details
- Recalling Firm
- MEDLINE INDUSTRIES, LP - Northfield
- Units Affected
- 56 kits
- Distribution
- US Nationwide distribution.
- Location
- Northfield, IL
Frequently Asked Questions
What product was recalled? ▼
MEDLINE KIT CV I II, REF DYNJ906071B. Recalled by MEDLINE INDUSTRIES, LP - Northfield. Units affected: 56 kits.
Why was this product recalled? ▼
Medline Industries, LP. has identified certain kits containing the recalled Medtronic lots of the DLP Vessel Cannulae. During manufacturing of the three listed lot numbers, product for model 30001 was incorrectly labeled as model 30000.
Which agency issued this recall? ▼
This recall was issued by the FDA Devices on October 23, 2024. Severity: Moderate. Recall number: Z-0123-2025.
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