OMNIlife science Inc. recalls
Every recall we track for OMNIlife science Inc. — 11 in all, from 2017–2020 — plus the complaints and injury reports the public filed about them.
Recalls per year, by danger level
Recalls from OMNIlife science Inc. peaked in 2019 (5); 11 since 2017.
All FDA recall records for OMNIlife science 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 | 0 | 1 | 0 | 1 |
| 2018 | 0 | 1 | 1 | 0 | 2 |
| 2019 | 0 | 2 | 3 | 0 | 5 |
| 2020 | 0 | 0 | 3 | 0 | 3 |
| 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 OMNIlife science 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 OMNIlife science Inc. recalls
7 shown- Lower riskMedical device
OMNIlife science Inc. recalls SERF Novae Dual Mobility Cup Insert 49/28-ApeX-LNK Poly Liner. Intended for use with the Apex Modular Acetabular Cup
OMNIlife recalls SERF Novae Dual Mobility Cup Insert 49/28-ApeX-LNK Poly Liner due to higher than acceptable oxidation limits, potentially requiring revision hip surgery.
OMNIlifeDec 21, 2020 - Lower riskMedical device
OMNIlife science Inc. recalls OMNI Hip System Model, Catalogue, or Order Number(s): HC-00070 Intended for use as the femoral component of a primary
OMNIlife recalls hip replacement model HC-00070 due to missing porous coating. This could affect bone integration. Affected users should contact for remedy.
OMNIlifeSep 11, 2019 - Lower riskMedical device
OMNIlife science Inc. recalls OMNIlife science, Inc. ApeX acetabular liner hip prosthesis component Serf Dual Mobility Cup Insert Liner 51-28;
OMNIlife science recalls ApeX acetabular liner hip prosthesis component Serf Dual Mobility Cup Insert Liner 51-28 due to potential higher wear rate leading to revision surgery.
OMNIlife scienceJul 23, 2019 - Use cautionMedical device
OMNIlife science Inc. recalls OMNIBotics iBlock Cutting Guide, 4146-1000 - Product Usage: The OMNIBotics iBlock Cutting Guide is a stainless-steel
OMNIlife recalls iBlock Cutting Guide 4146-1000 due to potential loosening during use. This surgical tool is used with robotic knee implants and may cause injury if not securely attached.
OMNIlifeApr 12, 2019 - Use cautionMedical device
OMNIlife science Inc. recalls OMNI K1 Broach Handle, Product Code HS-10054
OMNIlife recalls OMNI K1 Broach Handle (Product Code HS-10054) due to potential inner pin loosening and falling out. Affected units sold with Lot Number MM0118.
OMNIlifeNov 29, 2018 - Lower riskMedical device
OMNIlife science Inc. recalls OMNI Hip System, ApeX-LNK Acetabular Inserts 0 degree, 4+mm offset, Product Codes: H6-14436, H6-13928 & H6-14836
OMNIlife recalls hip implants with improperly labeled packaging. Affected products include Apex-LNK Acetabular Inserts for hip replacements. Consumers should check product codes and lot numbers for affected items.
OMNIlifeMay 18, 2018 - Lower riskMedical device
OMNIlife science Inc. recalls Apex Knee System, Tibial Baseplate Size 6 Left, non-porous - KC-2206L The Apex Knee System is intended for use as a
OMNIlife recalls Apex Knee System Tibial Baseplate Size 6 Left (KC-2206L) due to improper expiration date marked on external packaging. The correct expiration date is 2022-03, but the external packaging shows 2202-03. This may affect product safety.
OMNIlifeNov 20, 2017
OMNIlife science Inc. recall questions
How many recalls has OMNIlife science Inc. had?
11 recalls from OMNIlife science Inc. are on record with U.S. safety agencies, from 2017–2020.
What is the most recent OMNIlife science Inc. recall?
OMNIlife science Inc. recalls SERF Novae Dual Mobility Cup Insert 49/28-ApeX-LNK Poly Liner. Intended for use with the Apex Modular Acetabular Cup, dated Dec 21, 2020. Every OMNIlife science Inc. recall is listed on this page, newest first.
What should I do if I have a recalled OMNIlife science 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 OMNIlife science 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.