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Integra LifeSciences Corporation

Integra LifeSciences Corporation Recalls

All product recalls associated with Integra LifeSciences Corporation.

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Recall Summary

Total Recalls

1000

Past Year

1000

Class I (Serious)

145

Most Recent

Jan 2026

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 36161–36180 of 37661 recalls

Integra LifeSciences Corporation: MAYFIELD Radiolucent Disposable Adult Skull Pins (Sterile...

Skull pins, which fractured below device specifications during QC testing, were distributed.

FDAJun 29, 2004CO, MD, NY +1 more• Integra LifeSciences Corporation

Aaron Medical Industries, Inc.: Battery-operated Cautery High Temperature, fine/Loop/ Va...

The cover caps on some of these cauteries are not properly engaged to prevent inadvertent activation.

FDAJun 29, 2004IN• Aaron Medical Industries, Inc.

Aaron Medical Industries, Inc.: Battery-operated Cautery Low Temperature, fine/elongated...

The cover caps on some of these cauteries are not properly engaged to prevent inadvertent activation.

FDAJun 29, 2004IN• Aaron Medical Industries, Inc.

1...1807 180818091810 1811...1884

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Smiths Medical ASD, Inc.: Portex Hypodermic Needle-Pro Syringe and Needle 1ml/LS Sm...

Sterility of product is not assured

FDAJun 29, 2004Nationwide• Smiths Medical ASD, Inc.

Boston Scientific Corp: Boston Scientific brand Nephroureteral Stent System. Con...

Mislabeled as to size; 10FR are labeled as 8FR.

FDAJun 25, 2004MO• Boston Scientific Corp

Boston Scientific Corp: EMCEE OBTURATOR (7F) for use with 8F Sheath, REF #9258000...

Product labeled to contain Emcee Obturators contained Emcee Dilators.

FDAJun 24, 2004IN, NJ• Boston Scientific Corp

Varian Medical Systems Inc: medical device and software systems

a malfunction in the software of the VARiS versions 6.2.27 and 6.2.35 which is used to set up radiation therapy devices which will reset parameters to null for future treatments if a patient receives treatment on a non-varian machine and a varian machine and a non-varian field is loaded in the treatment session.

FDAJun 24, 2004Nationwide• Varian Medical Systems Inc

LG TM-510 Cell Phone Batteries (Verizon Wireless) – Battery Malfunction (2004)

Fire/Burn Risk

The recalled batteries can be found in LG TM-510 model cell phones, have a manufacturer/date code of "AEMLLL 02220," AEMMHH 02220," "AEMLLL 02X25H" or "AEMMHH 02725" and were distributed by Verizon Wireless. The manufacturer/date code can be found on the battery, below the words, "Model/Modelo" or "LG." The phone's model number appears on the back side of the phone beneath the battery. The cell phones, which come in black or silver, may have the Verizon Wireless name on the front.

CPSCJun 24, 2004Nationwide• Verizon Wireless of Bedminster, N.J.

Wheelbarrows (Ames) – Wheel Assembly Defect (2004)

Laceration Risk

The wheel assemblies on these wheelbarrows have a black plastic rim and have an approximately 14-inch diameter wheel. They have red, green, or orange tubs or trays made of steel or plastic and were sold under the brand names "Easy Roller," "Homeowner," "Mustang," or "Thoroughbred." The brand name was printed on the label attached to the tray at the time of purchase. Wheelbarrows with metal wheel assemblies are not part of this recall. No "True Temper" or "Jackson" wheelbarrow is part of this recall. In addition to the free replacement wheel assembly and free gardening tool incentive, the company is conducting the recall campaign with new measures to reach home gardeners who are the primary users of these recalled wheelbarrows. These new measures include placing ads in gardening publications, providing recall information to editors and webmasters of specialty gardening magazines and websites, and providing new point-of-sale posters to retailers.

CPSCJun 23, 2004Nationwide• O. Ames, a predecessor company of Ames True Temper Inc., of Camp Hill, Pa.

North Coast Medi-Tek Inc: E-Z-EM brand, Basic biopsy tray, catalog no. 4125.

Product contains the incorrect lot number.

FDAJun 23, 2004NY• North Coast Medi-Tek Inc

Osmetech Inc: Osmetech OPTI-CCA Blood Gas Analyzer, Single Use, BP7564 ...

In some cases patient samples with high glucose concentrations, above the reportable range of the OPTI-CCA Analyzer, may be erroneously reported as 'Low'.

FDAJun 22, 2004Nationwide• Osmetech Inc

Toddler Doll Family Sets (Lakeshore Learning) – Potential Hazard (2004)

Choking Hazard

The recall involves Toddler Doll Family sets sold with four figurines, a mom, dad, brother and sister. The 4-inch-tall dolls have a wooden head, arms and feet. The body is constructed of wire, which makes the doll adjustable. Each doll has yarn hair and is dressed in various colored outfits.

CPSCJun 22, 2004Nationwide• Lakeshore Learning Materials, of Carson, Calif.

Children's Swimsuit Cover-ups (Samara Brothers) – Unspecified Safety Concern (2004)

Choking Hazard

The recalled cover-ups were sold in various colors for boys and girls. Cover-ups were sold separately or as part of a swimsuit set. The cover-ups were sold under the brand names "Samara" and "Carter's," in sizes ranging from 3 to 24 months, 2T to 4T and 4X to 6X. On the short-sleeved cover-up are various patches depicting beach and swim-related themes. The name "Samara" or "Carter's" is printed on the garment-care tag, along with the size.

CPSCJun 22, 2004Nationwide• Samara Brothers Inc., of Edison, N.J.

Smith & Nephew Inc: Genesis Uni Articular Inserts

The firm received confirmed reports of Genesis Uni Articular Inserts not locking into tibial base plates intraoperatively.

FDAJun 21, 2004Nationwide• Smith & Nephew Inc

Smith & Nephew Inc: Tibial Base Plates

The firm received confirmed reports of Genesis Uni Articular Inserts not locking into tibial base plates intraoperatively.

FDAJun 21, 2004Nationwide• Smith & Nephew Inc

Toshiba American Med Sys Inc: Digital Radiography System, model DFP-8000D

Defect in the mirroring unit.

FDAJun 18, 2004Nationwide• Toshiba American Med Sys Inc

Spinal Specialties, Inc: Gertie Marx PainPak, Lot number 0504305, Reorder number 4060

Kit contains lidocaine, which has particulate matter in its ampule.

FDAJun 18, 2004MI, TX• Spinal Specialties, Inc

Spinal Specialties, Inc: Pencil Point Spinal Tray, Lot number 0504243

Kit contains lidocaine, which has particulate matter in its ampule.

FDAJun 18, 2004MI, TX• Spinal Specialties, Inc

Boston Scientific Corp: Boston Scientific/Microvasive brand Biliary Stent Kit, 7 ...

Mislabeled as to length; 10 cm length labeled as 5 cm.

FDAJun 18, 2004CA, HI, KY +2 more• Boston Scientific Corp

Boston Scientific Corp: Boston Scientific/MEDI-TECH brand Fascial Dilator, 8 FR(2...

Labeling mix-up as to product size; 8FR may be labeled 10FR and vice versa.

FDAJun 16, 2004Nationwide• Boston Scientific Corp