RegWardenFDA facility compliance records
Facility

ACCELERATED CARE PLUS CORP.

2 recall(s) on record — most severe on record: Class I.

Activity by year

FDA actions on record by year2013: 1 recalls; 2021: 1 recalls1’13’14’15’16’17’18’19’201’21’22’23’24’25’26
  • Recalls (2)

Devices registered here (1)

  • Diathermy, Shortwave, For Use In Applying Therapeutic Deep Heat
    Product code IMJ (opens in a new tab) · Class II · Physical Medicine · 21 CFR 890.5290

Recalls & enforcement

  • Class IOngoing2021-08-25
    Ultrasound gels and lotions manufactured by Eco-Med Pharmaceutical, Inc. may contain bacterial contamination. On August 18, 2021, FDA published a Letter to Health Care Providers to further address this issue: https://www.fda.gov/medical-devices/letters-health-care-providers/stop-…
  • Class IITerminated2013-06-12
    An anomaly in the firmware that may cause Omnicycle Elite to operate at a speed other than what was previously set when in reverse mode.

Related

Source: U.S. FDA via openFDA (opens in a new tab) (device registration & enforcement). Data as of 2026-10-06. Verify this facility record at FDA → (opens in a new tab)

Cite this record

RegWarden. “ACCELERATED CARE PLUS CORP. (FEI 1000119345) — FDA facility record.” Compiled from U.S. FDA public records (openFDA; FDA Data Dashboard). Data as of 2026-10-06. https://regwarden.com/facility/1000119345-accelerated-care-plus-corp/

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