Genicon, Inc. recalls
Every recall we track for Genicon, Inc. — 18 in all, from 2017–2020 — plus the complaints and injury reports the public filed about them.
Recalls per year, by danger level
Recalls from Genicon, Inc. peaked in 2018 (15); 18 since 2017.
All FDA recall records for Genicon, Inc. since 2017, counted by recall date (one bar per calendar year; 2026 is partial). Danger level is GovInfoNow’s plain-language rating; “not yet rated” records are still being written up.
| Year | Stop using now | Use caution | Lower risk | Not yet rated | Total |
|---|---|---|---|---|---|
| 2017 | 0 | 1 | 0 | 0 | 1 |
| 2018 | 0 | 4 | 11 | 0 | 15 |
| 2019 | 0 | 0 | 0 | 0 | 0 |
| 2020 | 0 | 1 | 0 | 1 | 2 |
| 2021 | 0 | 0 | 0 | 0 | 0 |
| 2022 | 0 | 0 | 0 | 0 | 0 |
| 2023 | 0 | 0 | 0 | 0 | 0 |
| 2024 | 0 | 0 | 0 | 0 | 0 |
| 2025 | 0 | 0 | 0 | 0 | 0 |
| 2026 (to date) | 0 | 0 | 0 | 0 | 0 |
What to do if you have a recalled Genicon, Inc. product
- Match the model, catalog or lot number on your device to the recall.
- Ask the prescribing clinician or supplier what to do — many device recalls are corrections, not removals.
- Report problems to FDA MedWatch.
All Genicon, Inc. recalls
5 shown- Use cautionMedical device
Genicon, Inc. recalls A Li-Gator Single Use Laparoscopic Clip Applier, 10 mm X 29 cm - Product Usage: intended for use on tubular structures
Genicon recalls single-use laparoscopic clip appliers (model 360-010-001) due to jamming and clip loading failures. Affected units sold with specific lot codes.
GeniconSep 17, 2020 - UnratedMedical device
Genicon, Inc. recalls Aquas PowerFlow Tube Set - Product Usage: The device delivers sterile irrigation fluids to surgical sites during
Genicon recalls Aquas PowerFlow Tube Sets due to lack of FDA premarket clearance. These surgical irrigation devices may not be safe for use during laparoscopic procedures.
GeniconAug 25, 2020 - Lower riskMedical device
Genicon, Inc. recalls Genicon GENILook Model 200-005-152, 5mm diameter, 100mm legnth (2 cannula, threaded) - Product Usage: The universal
Genicon recalls its GENILook Model 200-005-152 surgical device due to potential plastic tip detachment from metal shaft. Affected units sold with lot number I7717-C.
GeniconAug 21, 2018 - Lower riskMedical device
Genicon, Inc. recalls Genicon EZee Single Use Specimen Retrieval Bag - Product Usage: This device is disposable and is packaged and
Genicon recalls disposable specimen retrieval bags that may be used for multiple specimens, risking contamination. Affected units include model 550-000-00:000 with lot I8920 from August 2020.
GeniconJun 27, 2018 - Use cautionMedical device
Genicon, Inc. recalls GENICON EZEE Retrieval, sterile, Rx only.
Genicon recalls sterile EZEE Retrieval devices due to plastic handle breaking off, which can prevent proper removal. Affected units have specific catalog and lot numbers.
GeniconJul 19, 2017
Genicon, Inc. recall questions
How many recalls has Genicon, Inc. had?
18 recalls from Genicon, Inc. are on record with U.S. safety agencies, from 2017–2020.
What is the most recent Genicon, Inc. recall?
Genicon, Inc. recalls A Li-Gator Single Use Laparoscopic Clip Applier, 10 mm X 29 cm - Product Usage: intended for use on tubular structures, dated Sep 17, 2020. Every Genicon, Inc. recall is listed on this page, newest first.
What should I do if I have a recalled Genicon, Inc. product?
Match the model, catalog or lot number on your device to the recall. Ask the prescribing clinician or supplier what to do — many device recalls are corrections, not removals. Report problems to FDA MedWatch.
How do I get alerts for new Genicon, Inc. recalls?
Sign up for free email alerts on GovInfoNow — we check official CPSC, FDA, USDA and NHTSA data every day and email you only when a recall matches what you follow.