FDA recall record

DeRoyal SECURITY CUFFS, Single Strap, QR Buckle Cuff and Bed, UNIVERSAL, REF M8138 - Product recall — FDA Z-1604-2020

One lot of product was inadvertently manufactured with a buckle which does not meet the mechanical hold force required for this device.

Class IIclassification
Z-1604-2020official record ID
Apr 8, 2020report date

Recall record at a glance

Official recordZ-1604-2020
CategoryMedical Device Recalls
ClassificationClass II
FDA record statusTerminated
Recalling firmDeRoyal Industries Inc.
Report dateApr 8, 2020
Recall initiation dateFeb 27, 2020
Quantity94 pairs
LocationPowell, TN, United States

Official product description

DeRoyal SECURITY CUFFS, Single Strap, QR Buckle Cuff and Bed, UNIVERSAL, REF M8138 - Product Usage: patient restraint.

Why the product was recalled

One lot of product was inadvertently manufactured with a buckle which does not meet the mechanical hold force required for this device.

Distribution information

VA, CA, FL, AZ

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: E-Mail.

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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