Go Backs
HomeCategoriesStatesCheck Your Home
Go Backs

Track product recalls and safety alerts from CPSC, FDA, NHTSA, and USDA. Stay informed and keep your family safe.

Browse

  • Categories
  • States
  • Check Your Home
  • Risk Levels

Agencies

  • CPSC
  • FDA Food
  • FDA Drug
  • FDA Device
  • FDA Veterinary
  • NHTSA
  • USDA

Company

  • About
  • FAQ
  • Contact
  • Terms of Service
  • Privacy Policy
Buy Me a Coffee

Recall data is sourced from official U.S. government agencies (CPSC, FDA, NHTSA, USDA) and processed using AI to improve readability. This site is not affiliated with or endorsed by any government agency. Always refer to the original agency notice for authoritative information.

ยฉ 2026 Go Backs. All rights reserved.

Medium RiskFDA Device
Medical Devices/Surgical Equipment

Peter Lazic Gmbh: Aneurysm Clip Titanium Paddle-Clips Recalled for Incorrect Color Coding

Agency Publication Date: March 12, 2024
Share:
Sign in to monitor this recall

Summary

Peter Lazic Gmbh has recalled 221 units of its L-Aneurysm Clip TITANIUM Paddle-Clips because they were manufactured with the wrong color coding. These surgical clips, including 170 sterile units (Model S.45.782) and 51 non-sterile units (Model 45.782), feature blue paddle clips when they should have remained blank/uncolored. Because surgeons use color coding to identify the specific mechanical properties of these permanent implants, the incorrect color could lead to the selection of the wrong clip during a procedure. If you are a healthcare provider or patient who has received one of these clips, please contact the manufacturer or your hospital's surgical department immediately for guidance.

Risk

The incorrect blue coloring on these titanium clips may lead a surgeon to misidentify the device's technical specifications. This error could result in the application of a clip with unintended closing force or sizing during critical aneurysm surgery, potentially leading to surgical complications or device failure.

What You Should Do

  1. Check your surgical inventory for L-Aneurysm Clip TITANIUM Paddle-Clip (11 mm straight, permanent) with Model Numbers S.45.782 (Sterile) or 45.782 (Non-Sterile).
  2. Identify affected units by matching the following serial numbers: LX61400, LX61401, LX63366, LX63368 through LX63375, LX65981 through LX65984, LX66073 through LX66075, LX61372 through LX61395, LW50566 through LW50568, LX72845 through LX72854, LW36020 through LW36027, and UDI codes 04250603734697 or 04250603733799.
  3. Immediately inspect any matching clips for blue coloring on the paddle clips; if the paddles are blue instead of blank/silver, do not use the device.
  4. Isolate and quarantine all affected products to ensure they are not used in surgical procedures.
  5. Contact Peter Lazic Gmbh at their headquarters in Tuttlingen, Germany (Immelmannweg 2), or your local distributor to arrange for a replacement or further instructions regarding these units.
  6. If you are a patient who has recently undergone aneurysm surgery, consult with your surgeon or healthcare provider to discuss any concerns regarding the implants used during your procedure.
  7. For additional questions or to report issues, contact the FDA at 1-888-463-6332 or visit www.fda.gov/medical-devices/medical-device-recalls.

Your Remedy Options

๐Ÿ“‹Other Action

Manufacturer notification and correction

How to: Contact your healthcare provider or the manufacturer for further instructions and potential refund

Affected Products

Product: L-Aneurysm Clip TITANIUM Paddle-Clip, permanent, 11 mm straight, Sterile
Model / REF:
S.45.782
UPC Codes:
04250603734697
Lot Numbers (55):
LX61400
LX61401
LX63366
LX63368
LX63369
LX63370
LX63371
LX63372
LX63373
LX63374
LX63375
LX65981
LX65982
LX65983
LX65984
LX66073
LX66074
LX66075
LX61372
LX61373
LX61374
LX61375
LX61376
LX61377
LX61378
LX61379
LX61380
LX61381
LX61382
LX61383
LX61384
LX61385
LX61386
LX61387
LX61388
LX61389
LX61390
LX61391
LX61392
LX61393
LX61394
LX61395
LW50566
LW50567
LW50568
LX72845
LX72846
LX72847
LX72848
LX72849
Product: L-Aneurysm Clip TITANIUM Paddle-Clip, permanent, 11 mm straight, Non-Sterile
Model / REF:
45.782
UPC Codes:
04250603733799
Lot Numbers:
LX61385
LW36020
LW36021
LW36022
LW36023
LW36024
LW36025
LW36026
LW36027

Additional Information

Agency: Food and Drug Administration (FDA)
Event ID: 93952
Status: Active
Manufacturer: Peter Lazic Gmbh
Sold By: Medical facilities; Surgical centers
Manufactured In: Germany
Units Affected: 2 products (170 units; 51 units)
Distributed To: Maine

Were You Affected by This Recall?

If you or a family member were harmed by this recalled product, you may have legal rights. Consider consulting a consumer protection attorney to understand your options for compensation.

Find an Attorney

This is general information, not legal advice. Go Backs is not a law firm and does not provide legal services.

AI-Enhanced Content: The summary, action steps, and risk assessment on this page were generated by AI from official government recall data to improve readability. This is not legal or medical advice. Always refer to the official agency sources below for authoritative information.

Sources: FDA iRES ยท Raw API Response

openFDA Disclaimer: This recall information is sourced from the openFDA API. Do not rely on openFDA to make decisions regarding medical care. While we make every effort to ensure that data is accurate, you should assume all results are unvalidated. Refer to the openFDA terms of service for more information.