GREER LABORATORIES, INC.
1 recall(s) on record — most severe on record: Class II.
Activity by year
- Recalls (1)
- Inspections (2)
Devices registered here (1)
- Allergen And Vaccine Delivery NeedlesProduct code SCL (opens in a new tab) · Class II · General Hospital · 21 CFR 880.5570
Recalls & enforcement
- Class IITerminated2022-10-25The 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)
- NAI2022-11-01No Action Indicated · Compliance: Devices; Postmarket Assurance: Devices · citations posted
- NAI2017-06-15No 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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