Integrity Implants Inc. recalls
Every recall we track for Integrity Implants Inc. — 6 in all, from 2018–2024 — plus the complaints and injury reports the public filed about them. 1 is rated “stop using now”.
Recalls per year, by danger level
Recalls from Integrity Implants Inc. peaked in 2022 (4); 6 since 2017. 17% rated “stop using now”.
All FDA recall records for Integrity Implants 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 | 0 | 0 | 0 |
| 2018 | 0 | 0 | 1 | 0 | 1 |
| 2019 | 0 | 0 | 0 | 0 | 0 |
| 2020 | 0 | 0 | 0 | 0 | 0 |
| 2021 | 0 | 0 | 0 | 0 | 0 |
| 2022 | 1 | 0 | 0 | 3 | 4 |
| 2023 | 0 | 0 | 0 | 0 | 0 |
| 2024 | 0 | 0 | 1 | 0 | 1 |
| 2025 | 0 | 0 | 0 | 0 | 0 |
| 2026 (to date) | 0 | 0 | 0 | 0 | 0 |
What to do if you have a recalled Integrity Implants 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 Integrity Implants Inc. recalls
4 shown- Lower riskMedical device
Integrity Implants Inc. recalls Brand Name: N/A Product Name: Repeater Bone Tamp Model/Catalog Number: ASY-00132 Software Version: N/A Product
Integrity Implants recalls Repeater Bone Tamps (model ASY-00132, Rev A) due to incompatibility with bone funnels (Rev C). Affected users should contact the company for details.
Integrity ImplantsDec 20, 2024 - UnratedMedical device
Integrity Implants Inc. recalls LineSider Spinal System pedicle screws, 5.5/6.0mm, Non-mod Standard 7.1mm - Dual Lead, Non-cannulated. Model Number
Integrity Implants recalls LineSider Spinal System pedicle screws due to potential for screw head separation during surgery. Affected models include LS-N6SG6545. Consumers should contact the company for details.
Integrity ImplantsAug 3, 2022 - Stop using nowMedical device
Integrity Implants Inc. recalls LineSider Spinal System 5.5/6.0mm, Non-mod Standard 7.1mm - Dual Lead, Cannulated. Thoracolumbosacral pedicle screw
Integrity Implants recalls LineSider Spinal System screws for potential weld separation between components, which could lead to failure during spinal surgery. Affected units include specific sizes and lot numbers.
Integrity ImplantsJan 27, 2022 - Lower riskMedical device
Integrity Implants Inc. recalls FlareHawk Interbody Fusion System (previously XCage Interbody Fusion System) Instructions for Use (IFU's) only. Product
Integrity Implants recalls FlareHawk Interbody Fusion System Instructions for Use (IFU's) due to potential cleaning parameter discrepancies in labeling. Affected users should verify their IFU version and contact the company for updates.
Integrity ImplantsFeb 27, 2018
Integrity Implants Inc. recall questions
How many recalls has Integrity Implants Inc. had?
6 recalls from Integrity Implants Inc. are on record with U.S. safety agencies, from 2018–2024.
What is the most recent Integrity Implants Inc. recall?
Integrity Implants Inc. recalls Brand Name: N/A Product Name: Repeater Bone Tamp Model/Catalog Number: ASY-00132 Software Version: N/A Product, dated Dec 20, 2024. Every Integrity Implants Inc. recall is listed on this page, newest first.
What should I do if I have a recalled Integrity Implants 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 Integrity Implants 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.