Tuttlingen, N/A, Germany
Peter Lazic Gmbh recalls
2 recalls recorded since 2018, most recently on 6 October 2023. 2 are listed as ongoing. Status and classification are as published by the FDA.
Recalls2
Ongoing (FDA)2
Terminated or completed0
Class I (FDA)0
Ongoing Class II Medical devices
- Recall started
- 6 October 2023
- Reason
- Customer complaint received that reported the applier failed during surgery. The applier did not release the clip. The applier remained attached to the clip.
- Distribution
- US Nationwide distribution in the state of ME.
- Initiated
- Voluntary: Firm initiated
- Recall numbers
- Z-1279-2024, Z-1278-2024, Z-1277-2024
- D-Clip Standard/Mini Applier, 230mm bayonet, jaw rigid, double action.
- D-Clip Standard/Mini Applier, 210mm bayonet, jaw rigid, double action.
- D-Clip Standard/Mini Applier, 190mm bayonet, jaw rigid, double action.
Ongoing Class II Medical devices
- Recall started
- 14 July 2023
- Reason
- Wrong product coloring. The paddle clips should be blank, but they are colored blue.
- Distribution
- US Nationwide distribution in the state of ME.
- Initiated
- Voluntary: Firm initiated
- Recall numbers
- Z-1287-2024, Z-1288-2024
- L-Aneurysm Clip TITANIUM Paddle-Clip, permanent, 11 mm straight, Sterile
- L-Aneurysm Clip TITANIUM Paddle-Clip, permanent, 11 mm straight, Non-Sterile
A terminated FDA recall means the FDA has determined that all reasonable efforts to remove or correct the product have been made. What statuses mean.