FDA recall record

EMD Millipore Schiff Reagent, Hotchkiss-McManus, packaged in an amber glass bottle with a recall — FDA Z-1185-2024

This IVD is colorless. A customer complaint was received noting it appeared pink. A review of inventory confirmed additional stock appeared pink.

Class IIclassification
Z-1185-2024official record ID
Mar 6, 2024report date

Recall record at a glance

Official recordZ-1185-2024
CategoryMedical Device Recalls
ClassificationClass II
FDA record statusOngoing
Recalling firmEMD Millipore Corporation
Report dateMar 6, 2024
Recall initiation dateJan 26, 2024
Quantity106 Units (25 US, 81 OUS)
LocationBurlington, MA, United States

Official product description

Schiff Reagent, Hotchkiss-McManus, packaged in an amber glass bottle with a black polypropylene cap.

Why the product was recalled

This IVD is colorless. A customer complaint was received noting it appeared pink. A review of inventory confirmed additional stock appeared pink.

Distribution information

Domestic: AL, IL, MA, MN, NJ, PA, TX, VA. Foreign: Canada.

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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