NAFDAC: Deleject Disposable 21G Needles Recall Over Whitish Particulate Matter

• NAFDAC issued a public notice regarding Deleject Disposable 21G x 1 ½ Needles due to the presence of whitish particulate matter.
• The affected needles were manufactured with a date of June 2024 and are set to expire in May 2029.
• Healthcare professionals and distributors should verify the authenticity of these products and check for any further updates from NAFDAC.

The public notice was published on August 10, 2026, highlighting the importance of addressing this issue promptly.

A public notice was issued by the National Agency for Food and Drug Administration and Control (NAFDAC) regarding Deleject Disposable 21G x 1 ½ Needles, batch no. 240605. The notice followed an investigation into the presence of whitish particulate matter on these needles. This discovery has significant implications for patient safety, as the particulate matter may pose a risk to those using the affected needles.

The Deleject Disposable 21G x 1 ½ Needles in question were manufactured with a date of June 2024 and are set to expire in May 2029. The public notice was published on August 10, 2026, highlighting the importance of addressing this issue promptly.

The National Agency for Food and Drug Administration and Control (NAFDAC) is responsible for regulating food and drug products in Nigeria. As part of its mandate, NAFDAC ensures that all medical devices, including needles, meet the required standards before they are released to the market. The presence of whitish particulate matter on Deleject Disposable 21G x 1 ½ Needles raises concerns about the quality control measures in place for these products.

The recall and public notice issued by NAFDAC demonstrate the agency's commitment to protecting public health and safety. This action also underscores the importance of strict adherence to regulatory guidelines and standards in the manufacturing and distribution of medical devices.

Healthcare professionals and distributors play a crucial role in ensuring the authenticity and quality of medical devices used in patient care. The presence of whitish particulate matter on Deleject Disposable 21G x 1 ½ Needles highlights the need for vigilance in verifying the authenticity of these products.

NAFDAC's public notice serves as a reminder to all stakeholders involved in the healthcare supply chain to prioritize patient safety and adhere to regulatory guidelines. By doing so, they can prevent potential harm to patients and maintain trust in the medical devices used in their care.

Healthcare professionals and distributors should verify the authenticity of Deleject Disposable 21G needles and check for any further updates from NAFDAC regarding their use, as the presence of whitish particulate matter may pose a risk to patient safety.

Source: Original reporting via NAFDAC public notice