The Recall Desk

Manufacturer

DeRoyal Industries Inc

226 recalls in our database name DeRoyal Industries Inc as the manufacturing or recalling firm.

What the numbers show

Total
226
Critical
0
Severe
12
Most recent
2026-06-10

Of the 226 recalls from DeRoyal Industries Inc we have scored against our rubric, 0 (0%) are Critical — deaths or serious injuries reported, or the agency’s own highest classification — and 12 (5%) are Severe.

About this listing

The manufacturer string comes from the agency’s own source notice — for FDA recalls, the “recalling firm” field; for NHTSA recalls, the vehicle manufacturer; for CPSC recalls, the firm-of-record on the joint press release. A single corporate family can appear under multiple manufacturer strings as agency notices aren’t standardized on a canonical name. If you don’t see recalls you expect, try a parent-company search or a broader full-text search.

Severity scores below are computed from the agency’s classification and the recall text, never from manufacturer behaviour or history. Many manufacturers issue routine corrective actions (software updates, labelling corrections) that are correctly scored low — having recalls on this list isn’t inherently a quality signal.

26–50 of 226

  • HighFDA (Devices)·Z-0629-2023·2022-12-21

    Medical Device: DeRoyal HEART B PACK Recalled by FDA

    DeRoyal Industries initiated a Class II recall of its HEART B PACK medical device kit affecting 68 units distributed across 23 US states (Lot 56613762, expires 6/1/2026). The specific reason for recall is not available in source documentation.

    Product
    DeRoyal KIT HEART B PACK, REF 89-9042.07
    Category
    Medical Device
    Distribution
    23 states
  • HighFDA (Devices)·Z-0562-2023·2022-12-21

    DeRoyal Procedure Packs Recalled Due to Included 3M Steri Drapes

    DeRoyal Industries recalls EYE PACK procedure kits because they contain 3M Health Care Steri Drapes that have been recalled. The recall affects 156 kits distributed across 23 U.S. states.

    Product
    DeRoyal EYE PACK, REF 89-4051.09
    Category
    Medical Device
    Distribution
    23 states
  • HighFDA (Devices)·Z-0574-2023·2022-12-21

    FDA Class II recall: DeRoyal surgical procedure pack distributed to multiple states

    DeRoyal Industries voluntarily recalled 3 kits of its OPEN SHOULDER PROCEDURE PACK RF (Lot 56391733, expiring 3/1/2024) starting November 2022. The recall affects multiple U.S. states.

    Product
    DeRoyal OPEN SHOULDER PROCEDURE PACK RF, REF 89-6629.07
    Category
    Medical Device
    Distribution
    23 states
  • HighFDA (Devices)·Z-0708-2023·2022-12-21

    DeRoyal recalls Class II TRACECART POSTEROR LAMI MICRODISC device

    DeRoyal Industries is recalling 72 kits of TRACECART POSTEROR LAMI MICRODISC TRACECART devices distributed across 23 U.S. states in a voluntary Class II recall initiated by the manufacturer.

    Product
    DeRoyal TRACECART POSTEROR LAMI MICRODISC TRACECART, REF 53-1960.02
    Category
    Medical Device
    Distribution
    23 states
  • HighFDA (Devices)·Z-0662-2023·2022-12-21

    FDA Class II Recall: DeRoyal BIOPSY PACK Medical Device

    DeRoyal Industries has recalled 480 units of its BIOPSY PACK (REF 89-9614.07) in a voluntary, firm-initiated recall affecting 23 US states. The specific reason for the recall has not been disclosed.

    Product
    DeRoyal BIOPSY PACK, REF 89-9614.07
    Category
    Medical Device
    Distribution
    23 states
  • HighFDA (Devices)·Z-0680-2023·2022-12-21

    FDA recalls 90 DeRoyal pacemaker ICD device packs for defect

    DeRoyal Industries is recalling 90 kits of its Pacemaker ICD Pack (Lot 56705350, expiring June 1, 2026) distributed across 23 US states. The specific reason for this voluntary, firm-initiated recall is not disclosed in the FDA notice.

    Product
    DeRoyal PACEMAKER ICD PACK, REF 89-10216.03
    Category
    Medical Device
    Distribution
    23 states
  • HighFDA (Devices)·Z-0638-2023·2022-12-21

    FDA Class II recall of DeRoyal FOOT PACK medical devices

    DeRoyal Industries Inc has recalled 350 kits of the DeRoyal FOOT PACK medical device in a Class II FDA recall. The specific reason for the recall was not publicly disclosed in available agency records.

    Product
    DeRoyal FOOT PACK, REF 89-9252.06
    Category
    Medical Device
    Distribution
    23 states
  • HighFDA (Devices)·Z-0581-2023·2022-12-21

    DeRoyal Cannulated Hip Packs Recalled for Defective Steri Drapes

    DeRoyal Industries is recalling 108 kits of Cannulated Hip Procedure Packs because they contain 3M Steri Drapes that have been recalled. Affected lots were distributed across 23 U.S. states.

    Product
    DeRoyal CANNULTED HIP PACK CSM, REF 89-6977.09
    Category
    Medical Device
    Distribution
    23 states
  • HighFDA (Devices)·Z-0591-2023·2022-12-21

    DeRoyal procedure packs recalled for containing affected Steri Drapes

    DeRoyal Industries is recalling its BASIC NEURO PACK procedure packs because they contain 3M Health Care Steri Drapes that have been recalled. The recall affects 96 kits (lot 57287655, expires 9/1/2026) distributed to 23 states.

    Product
    DeRoyal BASIC NEURO PACK, REF 89-7258.12
    Category
    Medical Device
    Distribution
    23 states
  • HighFDA (Devices)·Z-0645-2023·2022-12-21

    Medical Device Recall: DeRoyal TOTAL KNEE PACK surgical kit

    DeRoyal Industries recalled 48 kits of the TOTAL KNEE PACK surgical product in November 2022. The specific reason for the recall was not disclosed in the public notice.

    Product
    DeRoyal TOTAL KNEE PACK, REF 89-9300.08
    Category
    Medical Device
    Distribution
    23 states
  • HighFDA (Devices)·Z-0711-2023·2022-12-21

    DeRoyal surgical cataract pack subject to Class II recall

    DeRoyal Industries voluntarily recalled 530 cataract surgical packs (Lot 57755800) classified as FDA Class II. The recall affects multiple U.S. states.

    Product
    DeRoyal CATARACT PACK, REF 89-8859.08
    Category
    Medical Device
    Distribution
    23 states
  • HighFDA (Devices)·Z-0580-2023·2022-12-21

    DeRoyal Cataract Procedure Packs Recalled Due to Defective Sterile Drapes

    DeRoyal Industries is recalling approximately 1,220 cataract procedure packs that contain recalled 3M Health Care Steri Drapes. The affected kits were distributed to healthcare facilities across 23 U.S. states.

    Product
    DeRoyal CATARACT PACK CSM, REF 89-6863
    Category
    Medical Device
    Distribution
    23 states
  • HighFDA (Devices)·Z-0609-2023·2022-12-21

    DeRoyal HEART PACK procedure kits recalled for defective component

    DeRoyal Industries is recalling 102 HEART PACK procedure kits (Lot 57367401, expiration 3/1/2025) distributed across 23 U.S. states because they contain recalled 3M Health Care Steri Drapes.

    Product
    DeRoyal HEART PACK, REF 89-8351.12
    Category
    Medical Device
    Distribution
    23 states
  • HighFDA (Devices)·Z-0667-2023·2022-12-21

    DeRoyal ACDF surgical implant kit recall, Class II, reason undisclosed

    DeRoyal is recalling 63 ACDF surgical implant kits distributed to 23 US states. This is a voluntary, Class II recall announced November 2022, with no reported illnesses or injuries.

    Product
    DeRoyal ACDF PACK PGYBK A PACK / B PACK, REF 89-9997.06
    Category
    Medical Device
    Distribution
    23 states
  • HighFDA (Devices)·Z-0626-2023·2022-12-21

    DeRoyal TLIF Procedure Packs Recalled Due to Included 3M Steri Drapes

    DeRoyal TLIF procedure packs containing recalled 3M Health Care Steri Drapes are being recalled. The affected packs were distributed across multiple U.S. states.

    Product
    DeRoyal TLIF PACK, REF 89-8780.04
    Category
    Medical Device
    Distribution
    23 states
  • HighFDA (Devices)·Z-0715-2023·2022-12-21

    DeRoyal Cataract Surgery Packs Recalled for Defective Components

    DeRoyal cataract procedure packs containing recalled 3M Health Care Steri Drapes are being recalled. The recall includes 520 kits distributed to healthcare facilities.

    Product
    DeRoyal CATARACT PACK, REF 89-10086.05
    Category
    Medical Device
    Distribution
    23 states
  • HighFDA (Devices)·Z-0695-2023·2022-12-21

    Hip replacement surgical kits recalled by DeRoyal Industries

    DeRoyal Industries Inc has recalled 19 anterior approach total hip replacement surgical kits distributed across 23 U.S. states. This Class II recall was initiated voluntarily by the manufacturer.

    Product
    DeRoyal ANTERIOR APPROACH TOTAL HIP A&B PGYBK, REF 89-10612.01
    Category
    Medical Device
    Distribution
    23 states
  • HighFDA (Devices)·Z-0655-2023·2022-12-21

    DeRoyal Shoulder Kit Subject to FDA Class II Recall

    DeRoyal Industries Inc is recalling 14 shoulder kits (Lot 56580884, expiring 12/1/2024) distributed to healthcare facilities in 23 states. The company initiated a voluntary Class II recall with the FDA.

    Product
    DeRoyal SHOULDER KIT, REF 89-9497.08
    Category
    Medical Device
    Distribution
    23 states
  • HighFDA (Devices)·Z-0560-2023·2022-12-21

    DeRoyal Minor Oral and ENT Procedure Packs Recalled for Defective Steri Drapes

    DeRoyal procedure packs distributed across multiple U.S. states are being recalled because they contain previously recalled 3M Steri Drapes. Affected healthcare facilities should stop using the packs and contact the manufacturer.

    Product
    DeRoyal MINOR ORAL / ENT PACK, REF 89-2576.15
    Category
    Medical Device
    Distribution
    23 states
  • HighFDA (Devices)·Z-0703-2023·2022-12-21

    FDA Medical Device Recall: DeRoyal Pacemaker ICD Pack

    DeRoyal Industries initiated a voluntary recall of its PACEMAKER ICD PACK (Lot 57805969, exp. 11/1/2026). The specific reason for recall is not provided in available source documentation. Affected units were distributed across 23 U.S. states.

    Product
    DeRoyal PACEMAKER ICD PACK, REF 89-10902.01
    Category
    Medical Device
    Distribution
    23 states
  • HighFDA (Devices)·Z-0561-2023·2022-12-21

    DeRoyal Oral Procedure Packs Recalled for Affected Steri Drapes

    DeRoyal Industries is recalling MAJOR ORAL PACK RF kits containing recalled 3M Health Care Steri Drapes. The affected lots were distributed to healthcare facilities in 23 US states.

    Product
    DeRoyal MAJOR ORAL PACK RF, REF 89-3936.15
    Category
    Medical Device
    Distribution
    23 states
  • HighFDA (Devices)·Z-0712-2023·2022-12-21

    DeRoyal Cataract Pack Surgical Kit Class II Recall

    DeRoyal Industries has recalled the DeRoyal CATARACT PACK (368 kits) in a voluntary Class II recall. Affected lot numbers are 55990451 and 56615717 with expiration 08/01/2024.

    Product
    DeRoyal CATARACT PACK, REF 89-9241.03
    Category
    Medical Device
    Distribution
    23 states
  • HighFDA (Devices)·Z-0670-2023·2022-12-21

    Surgical Spinal Fusion Device Recalled Across 23 US States

    DeRoyal is recalling its Posterior Lumbar Fusion Pack medical device across 23 states. The voluntary recall affects specific lot numbers; patients should consult their healthcare provider.

    Product
    DeRoyal POSTERIOR LUMBAR FUSION PACK, REF 89-10060.02
    Category
    Medical Device
    Distribution
    23 states

About this company

Community-sourced company facts from Wikidata, not from any recall agency. This is background on the corporate entity — it says nothing about the recall(s) listed on this page, which come from the agency source notice above.

DeRoyal

American healthcare company

Founded
1973

Official website

Source: Wikidata (Q5244070), licensed CC0. Wikidata is community-edited and may not reflect the current corporate structure.