RegWardenFDA facility compliance records
Facility

GREER LABORATORIES, INC.

1 recall(s) on record — most severe on record: Class II.

Activity by year

FDA actions on record by year2017: 1 inspections; 2022: 1 recalls, 1 inspections120172018201920202021220222023202420252026
  • Recalls (1)
  • Inspections (2)

Devices registered here (1)

  • Allergen And Vaccine Delivery Needles
    Product code SCL (opens in a new tab) · Class II · General Hospital · 21 CFR 880.5570

Recalls & enforcement

  • Class IITerminated2022-10-25
    The product was recalled because stability evaluation of the lots indicated a decrease in reactivity that could lead to a potential false-negative result interpretation. The issue was identified by the firm after failing to meet lot requirements for potency. The lot release erro…

FDA inspections (2)

  • NAI2022-11-01
    No Action Indicated · Compliance: Devices; Postmarket Assurance: Devices · citations posted
  • NAI2017-06-15
    No Action Indicated · Compliance: Devices; Postmarket Assurance: Devices · citations posted

Source: U.S. FDA Inspections Dashboard (opens in a new tab) (device inspection classifications, 2016–present). Data as of 2026-10-06. The dashboard profile can take several seconds to load.

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. “GREER LABORATORIES, INC. (FEI 1011574) — FDA facility record.” Compiled from U.S. FDA public records (openFDA; FDA Data Dashboard). Data as of 2026-10-06. https://regwarden.com/facility/1011574-greer-laboratories-inc/

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