Centurion Medical Products Corporation Diagnostic Imaging Tray (General Surgery convenience kit) Recall
Class II: A situation in which use of, or exposure to, a violative product may cause temporary or medically reversible adverse health consequences or where the probability of serious adverse health consequences is remote
Class II recall indicates potential for temporary health effects.
This AI-generated summary is provided for general informational purposes only and is derived from publicly available recall notices. It supplements but does not replace official agency classifications or safety instructions.
Check Your Product
According to the U.S. Food and Drug Administration (FDA)
Product
Diagnostic Imaging Tray (General Surgery convenience kit)
Brand
Centurion Medical Products Corporation
Lot Codes / Batch Numbers
CMP Kit code: MNS2955 Lot numbers: 2014061250 Expiration date: 2015-11
Products Sold
CMP Kit code: MNS2955 Lot numbers: 2014061250 Expiration date: 2015-11
Centurion Medical Products Corporation is recalling Diagnostic Imaging Tray (General Surgery convenience kit) due to According to the recall notice received from Hospira, the recall was initiated due to a confirmed customer report of particulate in a single unit. Hos. This is a Class I recall, indicating a high risk of serious health consequences or death. Based on FDA medical device enforcement report.
Summary derived from FDA notice
Reason for Recall
As stated by FDA
According to the recall notice received from Hospira, the recall was initiated due to a confirmed customer report of particulate in a single unit. Hospira identified the particulate as human hair, embedded in and attached to a pinched area of the stopper.
Recommended Action
Per FDA guidance
Healthcare providers and patients should stop using the device and contact the manufacturer for further instructions. Report problems to FDA MedWatch.
Verify this information on the official source
For complete details and official instructions, check the U.S. Food and Drug Administration (FDA) directly.
View official FDA recall noticePage updated: Jan 10, 2026