Stay Informed

Get email alerts when new recalls match your interests.

Recall data is updated hourly from official government sources. Very recent recalls may not yet appear. About our data sources

About

We make U.S. recall data searchable and accessible for consumers and businesses.

Site

FAQ
Browse by State
Statistics
Recall Classifications
About
Enterprise API

Legal

Privacy Policy
Terms of Service
Report Incorrect Info

Official Sources

FDA Recalls ↗
USDA FSIS ↗
CPSC Recalls ↗
NHTSA Recalls ↗

RSS Feed

Home
/
Brands
/
Integra LifeSciences Corp.

Integra LifeSciences Corp. Recalls

All product recalls associated with Integra LifeSciences Corp..

Get alerts for this brand

Recall Summary

Total Recalls

710

Past Year

Class I (Serious)

Most Recent

Dec 2025

Data from FDA, USDA, CPSC, and NHTSA public records. Recall counts vary by company size, industry, and reporting practices. Always check official sources for current information.

Showing 581–600 of 710 recalls

Integra LifeSciences Corp.: Integra Bilayer Matrix Wound Dressing, 8 in X 10 in (20 c...

Package Seal Integrity: Integra became aware of the potential of open seals in the foil pouch of the Integra Bilayer Matrix Wound Dressings.

FDAMar 10, 2009Nationwide• Integra LifeSciences Corp.

Edwards Lifesciences, Llc: Edwards Lifesciences Swan-Ganz Thermodilution Catheter RE...

Cardiac output measurements were unavailable and the following message is displayed in the Vigilance monitor: "Fault. CCO Catheter Verification. Use Bolus Mode".

FDAFeb 9, 2009AL, AZ, AR +37 more• Edwards Lifesciences, Llc

BD Biosciences, Systems & Reagents: BD FACSCount Controls Kit, An Automated Differential Cell...

The product is mislabeled, in that, zero/low controls were mislabeled as medium/high, and the medium/high controls were labeled zero/low.

FDA

1...28 293031 32...36

Page 30 of 36Next

Jan 29, 2009

Nationwide

• BD Biosciences, Systems & Reagents

Integra LifeSciences Corp: Integra Dermal Regeneration Template-TS Catalog number 32...

Potential for open seals in the inner foil pouch of certain products. The outer seal remains intact and therefore the sterility of the inner pouch is maintained.

FDAJan 16, 2009Nationwide• Integra LifeSciences Corp

Integra LifeSciences Corp: Integra Mosaik Putty, 15cc, Catalog # PTY10256 Integra Li...

Potential for open seals in the inner foil pouch of certain products. The outer seal remains intact and therefore the sterility of the inner pouch is maintained.

FDAJan 16, 2009Nationwide• Integra LifeSciences Corp

Imaging Sciences International, LLC: Gendex CB-500, 3D Dental Imaging Systems, Model Number G1...

faulty calibration

FDAJan 8, 2009FL, OH, PA• Imaging Sciences International, LLC

BD Biosciences, Systems & Reagents: BD FACS Sample Prep Assistant (SPA and SPA II) Instrument...

To prevent a needle stick while replacing the probe, the firm has initiated a Field Correction, and issued an improved Users Guide procedure (User Bulletin, Part Number 645050).

FDAJan 3, 2009Nationwide• BD Biosciences, Systems & Reagents

Edwards Lifesciences Research Medical, Inc.: CardioVations Ethicon, a Johnson and Johnson company, End...

Balloon rupture: Catheter balloon may rupture during cardiopulmonary bypass procedure. For further information, please telephone Edwards Lifesciences Research Medical, Inc. at 801-565-6173.

FDANov 26, 2008AL, AK, CA +32 more• Edwards Lifesciences Research Medical, Inc.

Edwards Lifesciences Research Medical, Inc.: Edwards Lifesciences CardioVations, EndoClamp aortic cath...

Balloon rupture: Catheter balloon may rupture during cardiopulmonary bypass procedure. For further information, please telephone Edwards Lifesciences Research Medical, Inc. at 801-565-6173.

FDANov 26, 2008AL, AK, CA +32 more• Edwards Lifesciences Research Medical, Inc.

BD Diagnostics (GeneOhm Sciences, Inc): BD Diagnostics, BD GeneOhm MRSA Assay, REF: 441242 (200 R...

BD Diagnostics GeneOhm (BDDG) has determined that the Cepheid SmartCycler reaction tubes packaged in the BD GeneOhm MRSA test kits identified above may be defective.

FDANov 11, 2008CA, IL, IN +15 more• BD Diagnostics (GeneOhm Sciences, Inc)

Integra LifeSciences Corp.: Integra Ruggles Surgical Instrument ACF Distraction Screw...

A packaging error had occurred where 16 mm screws were packaged and labeled as 12 mm screws and vice versa.

FDAOct 22, 2008Nationwide• Integra LifeSciences Corp.

Alnico Bar Magnets (Home Science Tools) – lead paint (2008)

This recall involves Alnico 3-inch long bar magnets. The magnets are painted red and blue, and were originally packaged as a pair or as a component of a science kit. The magnets were sold as item number MG-BAR3AL.

CPSCOct 14, 2008Nationwide• Home Science Tools, of Billings, Mont.

Cardiac Science Corporation: Cardio Vive 92532 AED, BURDICK Manufactured by Cardiac S...

Potential for AED to not deliver defibrillation therapy.

FDAOct 13, 2008PR• Cardiac Science Corporation

Cardiac Science Corporation: Cardiac Science First Save Automated External Defibrillat...

Potential for AED to not deliver defibrillation therapy.

FDAOct 13, 2008PR• Cardiac Science Corporation

Cardiac Science Corporation: Cardiac Science Powerheart Automated External Defibrillat...

Potential for AED to not deliver defibrillation therapy.

FDAOct 13, 2008PR• Cardiac Science Corporation

Cardiac Science Corporation: GE Responder 2019198 AED Manufactured for GE Medical Sys...

Potential for AED to not deliver defibrillation therapy.

FDAOct 13, 2008PR• Cardiac Science Corporation

Integra LifeSciences Corp.: Gravity Compensating Accessory; High Pressure Range, Ster...

Integra NeuroSciences has become aware that certain Gravity Compensating Accessory implants have the potential for CSF leakage under certain conditions.

FDAOct 3, 2008CA, IL, IN +3 more• Integra LifeSciences Corp.

Integra LifeSciences Corp: Uni-CP Compression Forceps (spreader); Non-sterile, R onl...

Reports of the Uni-CP Compression Forceps breaking during the Compression of the Uni-CP plate

FDASep 30, 2008Nationwide• Integra LifeSciences Corp

Edwards Lifesciences, Llc: Vigilance II Monitor Model: VIG2/VIG2E Software: versions...

Edwards Lifesciences has made the decision to initiate a field corrective action for the Edwards Vigilance II Model: Software: versions 00.51, 00.60, 00.61, 00.62, 00.63, 00.64, 00.67, 00.69, 00.71, 00.73 due to the potential of inaccurate Injectate Cardiac Output (ICO) measurements.

FDASep 12, 2008Nationwide• Edwards Lifesciences, Llc

Baxter Bioscience: FloSeal Endoscopic Applicator , Product Code 1500181. Th...

The recall is being conducted as a precautionary measure due to potential discoloration of the FloSeal material noted in six (6) non-medical complaints during delivery by the Endoscopic Applicator.

FDAJul 31, 2008Nationwide• Baxter Bioscience