Henry Schein recalls specific lots of Structur 2 SC Temporary Resin Cartridge Refills due to incorrect packaging and Instructions for Use from the FDA-cleared device. Affected units include product codes 114-3933 to 114-3937 with specific lot numbers.
Specific lots were distributed in the US with incorrect packaging and Instructions for Use (IFU) from the U.S. FDA-cleared device.
Henry Schein is recalling certain lots of Structur 2 SC Temporary Resin Cartridge Refills because they were distributed with incorrect packaging and Instructions for Use. This could lead to improper use of the dental material, potentially causing errors in dental procedures.
The recalled products were distributed with incorrect packaging and Instructions for Use (IFU) from the U.S. FDA-cleared device. This could lead to improper application of the dental material, potentially causing errors in temporary crown, bridge, inlay, or onlay procedures.
Dental professionals who use these specific lots of Structur 2 SC Temporary Resin Cartridge Refills are affected. The risk is low as the issue relates to packaging and instructions, not immediate safety hazards.
Check for product codes 114-3933 to 114-3937 with specific lot numbers: 2536179, 2606429; 2539064; 2533123; 2533203, 2607170. These are the affected lots of Structur 2 SC Temporary Resin Cartridge Refills.
Verify your product code and lot number against the listed affected lots to confirm if your item is recalled.
Henry Schein recalls specific lots of Structur 2 SC Temporary Resin Cartridge Refills due to incorrect packaging and Instructions for Use from the U.S. FDA-cleared device.
The recall record does not specify a remedy, so you should check the product details to confirm if your item is affected and contact Henry Schein for further guidance.
The recall indicates potential improper use due to incorrect packaging and instructions, but the hazard level is low as it does not involve immediate safety risks like injury or fire.
We’ve drafted a message you can send Henry Schein to request your refund or repair — edit it as you like.
Subject: Recall Z-3015-2026 — Henry Schein Henry Schein Hello, I own a Henry Schein that is covered by recall Z-3015-2026 from Henry Schein. I’m writing to arrange the remedy described in the recall (a refund, repair, or replacement as applicable). Could you please tell me the next steps to resolve this? Thank you.
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The facts (hazard, remedy, dates, manufacturer) are pulled from the official FDA recall record. The plain-language summary and step-by-step checklist are written by GovInfoNow to make the official notice easier to act on — they don’t replace it.
