Medline recalls sterile dental trays due to potential blade puncture of packaging foil. Affected items include Oral Surgery Packs and Extraction Packs with specific lot numbers.
Sterile blades within sterile kits have the potential for the blade to puncture the outer foil layer of the sterile packaging.
Medline is recalling sterile dental procedural trays that could have blades puncturing the outer foil packaging. This risk may lead to contamination of the sterile items during use.
Sterile blades inside the trays could puncture the outer foil layer of the packaging. This might cause contamination of the sterile items, potentially leading to infection risks during dental procedures.
Dental professionals and patients using the recalled sterile procedural trays. Those handling the specific lot numbers listed in the recall are most at risk.
Check for the following labels: ORAL SURGERY PACK-LF, EXTRACTION PACK, ORAL SURGERY PACK, or DENTAL MINOR PACK. Look for specific lot numbers: 22IDA002, 22HBR730, 22IDA539, 22HDB737, 22JBN386, 22KBG529, or 22JBO833.
Look for the product names listed in the recall: ORAL SURGERY PACK-LF, EXTRACTION PACK, ORAL SURGERY PACK, or DENTAL MINOR PACK.
Check the lot numbers on the packaging: 22IDA002, 22HBR730, 22IDA539, 22HDB737, 22JBN386, 22KBG529, or 22JBO834.
The recall states that sterile blades could puncture the foil packaging, but the product is not unsafe for use if the packaging remains intact. Users should check for the specific lot numbers listed.
The recall does not specify a remedy, so users should check the product labels and lot numbers to determine if they have affected items.
Check the product labels for the specific names (ORAL SURGERY PACK-LF, EXTRACTION PACK, etc.) and verify the lot numbers listed in the recall.
We’ve drafted a message you can send Medline Industries to request your refund or repair — edit it as you like.
Subject: Recall Z-1070-2023 — Medline Industries Medline Industries Hello, I own a Medline Industries that is covered by recall Z-1070-2023 from Medline Industries. 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.
