FDA recall record

DeRoyal Heart Cath Procedure Pack, REF 89-6556.08 recall — FDA Z-1833-2021

DeRoyal manufactured certain lots of surgical procedure pack products using Hospira Pfizer 1% Lidocaine which was subsequently recalled due to…

Class Iclassification
Z-1833-2021official record ID
Jun 16, 2021report date

Recall record at a glance

Official recordZ-1833-2021
CategoryMedical Device Recalls
ClassificationClass I
FDA record statusTerminated
Recalling firmDeRoyal Industries Inc.
Report dateJun 16, 2021
Recall initiation dateMay 14, 2021
Quantity66 packs
LocationPowell, TN, United States

Official product description

DeRoyal Heart Cath Procedure Pack, REF 89-6556.08

Why the product was recalled

DeRoyal manufactured certain lots of surgical procedure pack products using Hospira Pfizer 1% Lidocaine which was subsequently recalled due to mislabeling; the product is 0.5% Bupivacaine

Distribution information

US Nationwide distribution to the states of MS, VA, LA, and NY.

How to read the classification

FDA Class I indicates a situation in which there is a reasonable probability that use of or exposure to the product will cause serious adverse health consequences or death. The classification shown here comes directly from the FDA enforcement 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.

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.