Disclaimer: This site aggregates publicly available data from official government sources (FDA, ClinicalTrials.gov, PubMed, SEC EDGAR) for general reference only. It does NOT constitute medical advice, diagnosis, treatment recommendations, or investment advice.

Open, Classified

Healgen Series Reagent strips for Urinalysis are composed of several color pads aligned on a test strip. Each pad is employed for testing one assay item by visually or instrumentally reading the color change of the pad and comparing with the corresponding blocks on a color chart. The Healgen Series Reagent Strips for Urinalysis provides tests for Glucose, Bilirubin, Ketone, Specific Gravity, Blood, pH, Protein, Urobilinogen, Nitrite, Ascorbic Acid and Leukocytes in Urine.

FDA Recall Z-3303-2024 · Posted 2024-09-27

Recall StatusOpen, Classified
Product CodeJIR
Date Initiated2024-08-22
Product Quantity1,636,994 Tests

Reason for Recall

The reason for this recall is Healgen Scientific Ltd. has determined that their Urinary Reagent Strip products have shown reduced sensitivity, or potential false negative results for the detection of urinary protein by way of uneven color fading on the total protein test pad. This could lead to a delay in the identification of potential kidney diseases, their evaluation, and/or other conditions associated with elevated protein levels in urine and subsequently a delay in patient treatment.

Firm Action

On 08/22/2024, the firm sent an initial "URGENT MEDICAL DEVICE (IVD) RECALL" Letter to customer to inform them that, Urinary Reagent Strip products have shown reduced sensitivity and potential false negative results for Protein test. An updated communication will be issued on 08/28/2024. Customers are instructed to: -Immediately examine their inventory and quarantine products subject to recall. -Stop the sale of this product immediately. -Stop or cease use of the products immediately. -Recall products in the market. -Ship recalled products to Healgen's warehouse in Houston within 1 month of this notice (OR dispose of the product and provide proof of destruction (records, pictures, etc.) to Healgen.) -Use Appendix II to record the inventory report of the affected lots and send it back to Healgen. -Inform the end-user or sub-distributor at once of this recall and the required actions. Customers may request the unaffected replacement products from their local Healgen sales at no charge. Contact QA of Healgen Scientific, LLC at [email protected] or +1-713-733-8088 (Toll-Free) if you have any additional questions or concerns regarding this notification.

Root Cause

Nonconforming Material/Component

Distribution Pattern

U.S. Nationwide distribution in the states of CA, GA and TX.

Related FDA 510(k) Records

Devices referenced by this recall via K-numbers.

Official Source

View FDA Recall →

Source: FDA Enforcement Report / Recall database. Always confirm against the official FDA record.

↑