FDA recall record

DeRoyal KNEE BRACE, WARRIOR RECOVERY: 1) REF KB9000-01 2) REF 11-450A-00 3) REF 1150UTPP recall — FDA Z-0706-2020

The Warrior Recovery Knee Brace has the potential to come apart due to the hinge breaking.

Class IIclassification
Z-0706-2020official record ID
Dec 25, 2019report date

Recall record at a glance

Official recordZ-0706-2020
CategoryMedical Device Recalls
ClassificationClass II
FDA record statusOngoing
Recalling firmDeRoyal Industries Inc.
Report dateDec 25, 2019
Recall initiation dateNov 21, 2019
Quantity2789 units
LocationPowell, TN, United States

Official product description

DeRoyal KNEE BRACE, WARRIOR RECOVERY: 1) REF KB9000-01 2) REF 11-450A-00 3) REF 1150UTPP

Why the product was recalled

The Warrior Recovery Knee Brace has the potential to come apart due to the hinge breaking.

Distribution information

Nationwide, Australia, India, Saudi Arabia

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: Two or more of the following: Email, Fax, Letter, Press Release, Telephone, Visit.

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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