FDA recall record

Stryker Sustainability Solutions REF: 60-7070-005, Zimmer, Tourniquet Cuff 30" (Blue) recall — FDA Z-2405-2024

Mislabeling; tourniquet cuff packaging labeled as dual port single bladder but contains a tourniquet cuff single port single bladder.

Class IIclassification
Z-2405-2024official record ID
Jul 24, 2024report date

Recall record at a glance

Official recordZ-2405-2024
CategoryMedical Device Recalls
ClassificationClass II
FDA record statusOngoing
Recalling firmStryker Sustainability Solutions
Report dateJul 24, 2024
Recall initiation dateMay 31, 2024
Quantity90 units
LocationTempe, AZ, United States

Official product description

REF: 60-7070-005, Zimmer, Tourniquet Cuff 30" (Blue), Luer-Lock Dual Port, single Bladder, RxOnly

Why the product was recalled

Mislabeling; tourniquet cuff packaging labeled as dual port single bladder but contains a tourniquet cuff single port single bladder.

Distribution information

US Nationwide distribution in the states of CA, CO, IL, MI, OR, WI.

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

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