openFDA Device Enforcement
Report-date coverage
June 20, 2012–July 08, 2026
Known gap: openFDA describes 2004-present coverage, but the current export has no report-date records in this interval.
openFDA Device Recall
event_date_initiated coverage
June 01, 1997–June 30, 2026
Enforcement coverage uses report dates; product initiation dates can precede those bounds. Device-enrichment coverage uses FDA event_date_initiated.
Product dates, classifications, firms, and source wording remain attached to their individual rows.
Opening this dossier never hides products that did not match a prior timeline filter.
device · product 1 of 7
MEDLINE ADULT BLOOD CULTURE KIT, Reorder Number DYNDH1694A
Medline Industries, LP is issuing a recall for specific item(s) and lot(s) of Various Adult Blood and Blood Culture Kits. This recall is due to kits built using a Bactec component lot and expiration date that were not reflected on the kit insert. There is a risk of using an expired component if the user does not check the Bactec inside the kit for its expiration date.
These labels are deterministic app interpretations, not FDA categories.
Medline Industries, LP is issuing a recall for specific item(s) and lot(s) of Various Adult Blood and Blood Culture Kits. This recall is due to kits built using a Bactec component lot and expiration date that were not reflected on the kit insert. There is a risk of using an expired component if the user does not check the Bactec inside the kit for its expiration date.
Code information
UDI/DI 40195327139958 (case), 10195327139957 (unit), Lot Numbers: 23JBH262 and 23JBC264
Distribution pattern
US Nationwide distribution.
device · product 2 of 7
MEDLINE BLOOD CULTURE BOTTLE KIT, Reorder Number DYNDH1738A
Medline Industries, LP is issuing a recall for specific item(s) and lot(s) of Various Adult Blood and Blood Culture Kits. This recall is due to kits built using a Bactec component lot and expiration date that were not reflected on the kit insert. There is a risk of using an expired component if the user does not check the Bactec inside the kit for its expiration date.
These labels are deterministic app interpretations, not FDA categories.
Medline Industries, LP is issuing a recall for specific item(s) and lot(s) of Various Adult Blood and Blood Culture Kits. This recall is due to kits built using a Bactec component lot and expiration date that were not reflected on the kit insert. There is a risk of using an expired component if the user does not check the Bactec inside the kit for its expiration date.
Code information
UDI/DI 40195327239849 (case), 10195327239848 (unit), Lot Numbers: 23JBM366
Distribution pattern
US Nationwide distribution.
device · product 3 of 7
MEDLINE BLOOD CULTURE COLLECTION KIT, Reorder Number DYNDH1714A
Medline Industries, LP is issuing a recall for specific item(s) and lot(s) of Various Adult Blood and Blood Culture Kits. This recall is due to kits built using a Bactec component lot and expiration date that were not reflected on the kit insert. There is a risk of using an expired component if the user does not check the Bactec inside the kit for its expiration date.
These labels are deterministic app interpretations, not FDA categories.
Medline Industries, LP is issuing a recall for specific item(s) and lot(s) of Various Adult Blood and Blood Culture Kits. This recall is due to kits built using a Bactec component lot and expiration date that were not reflected on the kit insert. There is a risk of using an expired component if the user does not check the Bactec inside the kit for its expiration date.
Code information
UDI/DI 40195327347551 (case), 10195327347550 (unit), Lot Numbers: 23KBC138
Distribution pattern
US Nationwide distribution.
device · product 4 of 7
MEDLINE BLOOD CULTURE COLLECTION KIT, Reorder Number DYNDH1626B
Medline Industries, LP is issuing a recall for specific item(s) and lot(s) of Various Adult Blood and Blood Culture Kits. This recall is due to kits built using a Bactec component lot and expiration date that were not reflected on the kit insert. There is a risk of using an expired component if the user does not check the Bactec inside the kit for its expiration date.
These labels are deterministic app interpretations, not FDA categories.
Medline Industries, LP is issuing a recall for specific item(s) and lot(s) of Various Adult Blood and Blood Culture Kits. This recall is due to kits built using a Bactec component lot and expiration date that were not reflected on the kit insert. There is a risk of using an expired component if the user does not check the Bactec inside the kit for its expiration date.
Code information
UDI/DI 40195327323333 (case), 10195327323332 (unit), Lot Numbers: 23KBH642
Distribution pattern
US Nationwide distribution.
device · product 5 of 7
MEDLINE BLOOD CULTURE KIT, Reorder Number DYNDH1723
Medline Industries, LP is issuing a recall for specific item(s) and lot(s) of Various Adult Blood and Blood Culture Kits. This recall is due to kits built using a Bactec component lot and expiration date that were not reflected on the kit insert. There is a risk of using an expired component if the user does not check the Bactec inside the kit for its expiration date.
These labels are deterministic app interpretations, not FDA categories.
Medline Industries, LP is issuing a recall for specific item(s) and lot(s) of Various Adult Blood and Blood Culture Kits. This recall is due to kits built using a Bactec component lot and expiration date that were not reflected on the kit insert. There is a risk of using an expired component if the user does not check the Bactec inside the kit for its expiration date.
Code information
UDI/DI 40195327134205 (case), 10195327134204 (unit), Lot Numbers: 23JBO541
Distribution pattern
US Nationwide distribution.
device · product 6 of 7
MEDLINE BLOOD CULTURE KIT, Reorder Number DYNDH1622C
Medline Industries, LP is issuing a recall for specific item(s) and lot(s) of Various Adult Blood and Blood Culture Kits. This recall is due to kits built using a Bactec component lot and expiration date that were not reflected on the kit insert. There is a risk of using an expired component if the user does not check the Bactec inside the kit for its expiration date.
These labels are deterministic app interpretations, not FDA categories.
Medline Industries, LP is issuing a recall for specific item(s) and lot(s) of Various Adult Blood and Blood Culture Kits. This recall is due to kits built using a Bactec component lot and expiration date that were not reflected on the kit insert. There is a risk of using an expired component if the user does not check the Bactec inside the kit for its expiration date.
Code information
UDI/DI 40195327509874 (case), 10195327509873 (unit), Lot Numbers: 23JBQ525
Distribution pattern
US Nationwide distribution.
device · product 7 of 7
MEDLINE BLOOD CULTURE TRAY ADULT, Reorder Number DYNDH1194A
Medline Industries, LP is issuing a recall for specific item(s) and lot(s) of Various Adult Blood and Blood Culture Kits. This recall is due to kits built using a Bactec component lot and expiration date that were not reflected on the kit insert. There is a risk of using an expired component if the user does not check the Bactec inside the kit for its expiration date.
These labels are deterministic app interpretations, not FDA categories.
Medline Industries, LP is issuing a recall for specific item(s) and lot(s) of Various Adult Blood and Blood Culture Kits. This recall is due to kits built using a Bactec component lot and expiration date that were not reflected on the kit insert. There is a risk of using an expired component if the user does not check the Bactec inside the kit for its expiration date.
Code information
UDI/DI 40195327432301 (case), 10195327432300 (unit), Lot Numbers: 23JBO540
