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Oklahoma Blood Institute Coffee Memorial Blood Center FDA Inspection Record

FEI 1671267 · Inspections, Form 483s, warning letters and import refusals

Oklahoma Blood Institute Coffee Memorial Blood Center is an FDA-inspected facility (FEI 1671267) located in Amarillo, TX, US. RegDataLab tracks 6 FDA inspections at this facility.

What FDA found at this site

Latest inspection: Mar 24, 2025: No Action Indicated (NAI)
Inspections on record: 6 (6 NAI)
Last OAI inspection: None on record
Warning letters: None matched to this FEI. Many letters do not state an FEI: search warning letters by company name
Recalls as the recalling firm: 16, latest Aug 16, 2013

A Form 483 lists an inspector's observations. OAI means FDA recommends regulatory and/or administrative action. A warning letter is FDA's formal enforcement notice. No record here does not establish that a site is safe. Check this site on FDA's Data Dashboard.

Inspections and what FDA cited

Newest first. Citations are the inspector observations FDA publishes for the inspection.

Date	Result	What FDA cited
Mar 24, 2025	No Action Indicated (NAI)	No citations listed
Sep 13, 2019	No Action Indicated (NAI)	No citations listed
May 9, 2017	No Action Indicated (NAI)	No citations listed
Mar 25, 2015	No Action Indicated (NAI)	No citations listed
Jan 8, 2013	No Action Indicated (NAI)	No citations listed
Feb 4, 2011	No Action Indicated (NAI)	No citations listed

Recalls

Showing the 10 most recent of 16 recalls. Recalls FDA's Enforcement Report lists with this FEI as the recalling firm. The recalling firm is not always the site that made the product. Search FDA's Enforcement Report by recall number.

Date	Class	Recall	Product and reason
Aug 16, 2013	Class II	B-0239-14	Blood and Blood Products for Reprocessing and 1 more product Blood products, collected from a donor whose suitability to donate was not adequately determined, were distributed.
Jul 29, 2013	Class II	B-0032-14	Red Blood Cells Leukocytes Reduced and 1 more product Blood products, collected from a donor whose suitability to donate was not adequately determined, were distributed.
May 16, 2013	Class III	B-2359-13	Blood and Blood Products for Reprocessing Blood product, which was collected from a donor in which donor suitability was not adequately determined, was distributed.
Nov 21, 2012	Class II	B-1018-13	Red Blood Cells Leukocytes Reduced Blood product, collected from a donor who received a tattoo within 12 months of donation, were distributed.
Apr 16, 2011	Class II	B-0415-13	Platelets Leukocytes Reduced and 1 more product Blood products, for which the sterility may have been compromised, were distributed.
Mar 23, 2005	Class II	B-0694-6	Red Blood Cells Leukocytes Reduced Blood product, collected from a donor whose suitability to donate was not adequately determined, was distributed.
Mar 21, 2005	Class II	B-0752-6	Red Blood Cells, Leukocytes Reduced and 1 more product Blood products, which tested negative for hepatitis, but were collected from a donor with a history of Hepatitis A, were distributed.
Feb 3, 2005	Class II	B-0700-6	Red Blood Cells, Leukocytes Reduced Blood product, labeled with an incorrect expiration date, was distributed.
Jan 6, 2005	Class II	B-0758-6	Red Blood Cells, Leukocytes Reduced, Irradiated and 1 more product Blood products, for which documentation of irradiation was incomplete, were distributed.
Dec 9, 2004	Class II	B-0751-6	Platelets Pheresis, Leukocytes Reduced, Irradiated Blood product, which was incorrectly labeled as having been irradiated, was distributed.

FDA record score

0 of 100. A count of this site's adverse public FDA records, weighted by how recent each one is. A higher number means more, or more recent, records. Each record below adds the points shown.

Counted on Nov 14, 2026, method version 1. It counts records and does not judge the site: a low number does not establish that a site is safe, and sites that FDA inspects more often can collect more points. How this is counted.

12 records behind this number

Record	Date	Points x age weight
Class II recall B-0239-14, this FEI as the recalling firm	Aug 16, 2013	10 years or older, so it adds no points
Class II recall B-0032-14, this FEI as the recalling firm	Jul 29, 2013	10 years or older, so it adds no points
Class II recall B-1018-13, this FEI as the recalling firm	Nov 21, 2012	10 years or older, so it adds no points
Class II recall B-0415-13, this FEI as the recalling firm	Apr 16, 2011	10 years or older, so it adds no points
Class II recall B-0694-6, this FEI as the recalling firm	Mar 23, 2005	10 years or older, so it adds no points
Class II recall B-0752-6, this FEI as the recalling firm	Mar 21, 2005	10 years or older, so it adds no points
Class II recall B-0700-6, this FEI as the recalling firm	Feb 3, 2005	10 years or older, so it adds no points
Class II recall B-0758-6, this FEI as the recalling firm	Jan 6, 2005	10 years or older, so it adds no points
Class II recall B-0751-6, this FEI as the recalling firm	Dec 9, 2004	10 years or older, so it adds no points
Class II recall B-1665-3, this FEI as the recalling firm	Mar 6, 2003	10 years or older, so it adds no points
Class II recall B-1666-3, this FEI as the recalling firm	Jan 8, 2003	10 years or older, so it adds no points
Class II recall B-1571-3, this FEI as the recalling firm	May 31, 2002	10 years or older, so it adds no points

When each source was last refreshed

FDA sources behind this page and when RegDataLab last refreshed each one
Records	Last refreshed	Source as of	Status
Inspections	Nov 14, 2026	Newest record Nov 5, 2026	Current
Inspection citations	Nov 14, 2026	Newest record Nov 5, 2026	Current
Compliance actions (warning letters, injunctions and other action types)	Nov 2, 2026	Newest record Oct 29, 2026	Current
Warning letter text	Nov 14, 2026	Newest record Nov 10, 2026	Current
Recalls (Enforcement Report)	Nov 14, 2026	Newest record Nov 11, 2026	Current
Form 483s and inspection documents	Nov 13, 2026	Newest record Nov 12, 2026	Current
Import refusals	Nov 2, 2026	Newest record Oct 22, 2026	Current

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Facility details

Company: Oklahoma Blood Institute Coffee Memorial Blood Center
Location: Amarillo, TX (US)
Source: inspections