Recall Z-0534-2025— MEDLINE INDUSTRIES, LP - Northfield
Class II · Ongoing
Class II FDA medical device recall by MEDLINE INDUSTRIES, LP - Northfield, initiated 2024-10-15. FDA's recall record names no specific 510(k) clearance for this event. Product: Medline Shoulder Repair Pack-LF, REF DYNJ82607, 2 kits/case, sterile.. Reason: Some of the suture packages within the convenience kits contain the incorrect needle type/size and suture diameter/length..
- Recalling firm
- MEDLINE INDUSTRIES, LP - Northfield
- Classification
- Class II
- Status
- Ongoing
- Initiated
- 2024-10-15
- Firm location
- Northfield, IL, United States
Product description
Medline Shoulder Repair Pack-LF, REF DYNJ82607, 2 kits/case, sterile.
Reason for recall
Some of the suture packages within the convenience kits contain the incorrect needle type/size and suture diameter/length.
Data sourced from openFDA. This site is unofficial and independent of the FDA.