FDA recall record

Kerr/Pentron, DBA Kerr Corporation and Pentron Regimen 28 Day - Glutaraldehyde Sterilizing recall — FDA Z-1721-2019

Immersion time stated on the bottle is 45 minutes while the product instructions say 90 minutes.

Class IIclassification
Z-1721-2019official record ID
Jun 12, 2019report date

Recall record at a glance

Official recordZ-1721-2019
CategoryMedical Device Recalls
ClassificationClass II
FDA record statusTerminated
Recalling firmKerr/Pentron, DBA Kerr Corporation and Pentron Clinical
Report dateJun 12, 2019
Recall initiation dateJul 13, 2018
Quantity31904
LocationOrange, CA, United States

Official product description

Regimen 28 Day - Glutaraldehyde Sterilizing and Disinfecting Solution

Why the product was recalled

Immersion time stated on the bottle is 45 minutes while the product instructions say 90 minutes.

Distribution information

AZ, CA, CO, FL, GA, IL, KY, LA, MA, MN, MO, NJ, NY, OH, PA, SC, TN, TX, UT, VA, and WA.

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.

FDA source limitation: openFDA enforcement reports are a reference dataset, not a live public-alert or recall-lifecycle service. FDA notes that enforcement-report status may not be updated after classification. Confirm current actions with the FDA, recalling firm or appropriate healthcare professional when relevant.

Related recall records

Other records from the same recalling company are shown first when available.