Recall Z-2711-2024— MEDLINE INDUSTRIES, LP - Northfield
Class II · Ongoing
Class II FDA medical device recall by MEDLINE INDUSTRIES, LP - Northfield, initiated 2024-03-22. FDA's recall record names no specific 510(k) clearance for this event. Product: Medline medical procedure kits labeled as follows: a) BASIC NEURO, REF DYNJ909171A; b) NEURO, REF DYNJ905510D; c) NEURO, REF DYNJ902388L; d) NEURO SAS, REF DYNJ908566. Reason: A slight dimensional variation which has the potential for increased difficulty fitting into outer canister..
- Recalling firm
- MEDLINE INDUSTRIES, LP - Northfield
- Classification
- Class II
- Status
- Ongoing
- Initiated
- 2024-03-22
- Firm location
- Northfield, IL, United States
Product description
Medline medical procedure kits labeled as follows: a) BASIC NEURO, REF DYNJ909171A; b) NEURO, REF DYNJ905510D; c) NEURO, REF DYNJ902388L; d) NEURO SAS, REF DYNJ908566
Reason for recall
A slight dimensional variation which has the potential for increased difficulty fitting into outer canister.
Data sourced from openFDA. This site is unofficial and independent of the FDA.