FDA recall record

Ansell Healthcare Products GAMMEX NON-LATEX PI GREEN Surgical gloves, REF: 20685255 through recall — FDA Z-0096-2024

Some surgical glove sterile pouches were not completely sealed.

Class IIclassification
Z-0096-2024official record ID
Oct 18, 2023report date

Recall record at a glance

Official recordZ-0096-2024
CategoryMedical Device Recalls
ClassificationClass II
FDA record statusOngoing
Recalling firmAnsell Healthcare Products LLC
Report dateOct 18, 2023
Recall initiation dateAug 3, 2023
Quantity1511
LocationReno, NV, United States

Official product description

GAMMEX NON-LATEX PI GREEN Surgical gloves, REF: 20685255 through 20685290

Why the product was recalled

Some surgical glove sterile pouches were not completely sealed.

Distribution information

Worldwide - US Nationwide distribution in the states of IN, OH, NY, VA, IL, TN, GA, NY, SC, WI, FL and the country of CA.

How to read the classification

FDA Class II indicates a situation in which use of or exposure to the product may cause temporary or medically reversible adverse health consequences, or where the probability of serious consequences is remote. The classification shown here comes from the FDA record.

Additional record details

Recall type: Voluntary: Firm initiated. Initial notification: Letter.

What to do next

If you believe you have the recalled product, use the recall number and firm information above to confirm the official notice and follow the instructions issued by the FDA, recalling firm, retailer or product manufacturer. For drugs and medical devices, decisions about treatment or medical care should be discussed with a qualified health professional.

About this record

Recall Lookup USA preserves the most complete source information successfully retrieved. We do not create missing facts or infer affected lots or VINs. The official record may still change, so use the identifier above when verifying current instructions.

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