Certified Safety Mfg Inc recalls first aid kits and cabinets containing Medi-First XS Non-Aspirin and Sinus Pain & Pressure products due to cGMP deviations at the manufacturer. Affected items include specific model numbers and lot numbers.
First aid kit and cabinet components are being recalled by the supplier due to cGMP deviations at the manufacturer.
Certified Safety Mfg Inc is recalling first aid kits and cabinets that contain Medi-First XS Non-Aspirin and Sinus Pain & Pressure products. The recall is due to manufacturing deviations that may affect product safety standards.
The recall is based on cGMP (Current Good Manufacturing Practice) deviations at the manufacturer. This means the products may not meet safety standards, but the specific hazard mechanism is not clearly described in the recall notice.
First aid kits and cabinets with specific model numbers and lot numbers from the manufacturer's list are affected. Individuals using these products in workplaces or homes may be at risk.
Check for model numbers like K614-020, KR614-020, K616-033, and lot numbers such as 6348 for Medi-First XS Non-Aspirin products. The recall includes specific box and packet lot numbers listed in the notice.
Review the model numbers and lot numbers listed in the recall notice to confirm if your first aid kit or cabinet is affected.
The recall is due to cGMP deviations at the manufacturer, which may affect product safety standards.
The recall notice does not specify a remedy, so check the model numbers and lot numbers to determine if your product is affected.
Look for model numbers like K614-020, KR614-020, K616-033, and lot numbers such as 6348 for Medi-First XS Non-Aspirin products as listed in the recall notice.
We’ve drafted a message you can send Certified Safety Mfg Inc to request your refund or repair — edit it as you like.
Subject: Recall Z-1060-2022 — Certified Safety Mfg Inc Certified Safety Mfg Inc Hello, I own a Certified Safety Mfg Inc that is covered by recall Z-1060-2022 from Certified Safety Mfg Inc. 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.
