State

Oklahoma product recalls

73,722 recalls have nationwide distribution and so reach Oklahoma. 5,822 additional recalls listed Oklahoma specifically in their distribution scope.

What the numbers show

Total: 5,822
Critical: 1,040
Severe: 1,493
Most recent: 2026-10-28

Of the 5,822 recalls naming Oklahoma we have scored against our rubric, 1,040 (18%) are Critical — deaths or serious injuries reported, or the agency’s own highest classification — and 1,493 (26%) are Severe.

Which agencies issued them

These figures cover only the 5,822 recalls whose distribution notice names Oklahoma specifically. The 73,722 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.

31426–31450 of 79544

SevereFDA (Drugs)·D-1091-2020·2020-04-15
PharMEDium Recalls ePHEDrine Sulfate Syringes Due to Sterility Assurance Issues
PharMEDium Services is recalling 46 lots of ePHEDrine Sulfate syringes because of a lack of sterility assurance. The products were distributed nationwide in the US.
Product
ePHEDrine Sulfate 10 mg per mL 50 mg per 5 mL in 0.9% 5 mL Sodium Chloride 5 mL syringe, For IV Use, Rx Only, PharMEDium 913 N Davis Avenue Cleveland, MS NDC 71030-001-09
Category
Drug
Distribution
Distributed nationwide
SevereFDA (Drugs)·D-1104-2020·2020-04-15
Avet Pharmaceuticals Recalls Losartan Potassium Tablets Due to Impurity
Avet Pharmaceuticals is recalling Losartan Potassium Tablets 100 mg because FDA labs found an impurity above acceptable levels.
Product
Losartan Potassium Tablets USP 100 mg, supplied in a) 30 count (NDC 23155-646-03, b) 90 count (NDC 23155-646-09) and 1000 count (NDC 23155-646-10) bottles, Rx only, Manufactured by: Vivimed Life Sciences Private Limited, Tamil Nadu, India Manufactured for: Heritage…
Category
Drug
Distribution
Distributed nationwide
SevereFDA (Devices)·Z-1677-2020·2020-04-15
Siemens ARTISTE MV System Recalled for Radiation Dose Monitoring Safety Interlock Defect
Siemens is recalling ARTISTE MV Systems due to a potential safety issue with dose monitoring interlocks that could result in a 10-20% radiation therapy overdose.
Product
ARTISTE MV System Model #8139789 with Digital LINAC Systems Control Console Software Versions 6, 7, 9, 13
Category
Medical Device
Distribution
35 states
SevereFDA (Drugs)·D-1087-2020·2020-04-15
PharMEDium Recalls Rocuronium Bromide Syringes Due to Sterility Assurance Issues
PharMEDium Services, LLC is recalling 46 lots of rocuronium bromide syringes because of a lack of sterility assurance. The products were distributed nationwide in the US.
Product
rocuronium Bromide, 10 mg per mL, 50 mg per 5 mL, 5 mL BD Syringe, for IV Use, PharMEDium 13N. Davis Ave. Cleveland MS 36732. NDC 71019-321-05
Category
Drug
Distribution
Distributed nationwide
SevereFDA (Drugs)·D-1093-2020·2020-04-15
PharMEDium Recalls Fentanyl Citrate Injection Due to Sterility Assurance Issues
PharMEDium Services, LLC is recalling 46 lots of fentanyl citrate injection products because of a lack of sterility assurance.
Product
fentaNYL Citrate Injection 50 mcg per mL, 100 mcg per 2 mL, 2 mL per syringe, For IV Use, Rx Only, PharMEDium Services, LLC 913 N. Davis Ave Cleveland, MS 05810. NDC 61553-303-28
Category
Drug
Distribution
Distributed nationwide
SevereFDA (Drugs)·D-1085-2020·2020-04-15
PharMEDium Recalls Fentanyl Citrate Infusions Due to Sterility Assurance Issues
PharMEDium Services, LLC is recalling 46 lots of fentanyl citrate infusions because of a lack of sterility assurance. The products were distributed nationwide in the US.
Product
fentaNYL Citrate 10 mcg per mL, 2,500 mcg per 250 mL, 250 mL in a LifeCare Bag, in Sodium Chloride 0.9%. Rx Only, PharMEDium Services, LLC 913 N. Davis Ave Cleveland, MS 36732 NDC 61553-113-50
Category
Drug
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1684-2020·2020-04-15
Radiometer ABL800 FLEX Blood Gas Analyzer Barcode Reader Recall
Radiometer Medical ApS is recalling ABL800 FLEX analyzers because the barcode reader may misinterpret labels, potentially causing patient mixups or sample loss.
Product
ABL800 FLEX, model number/UDI 393-800/0570 In Vitro testing of samples of whole blood for the parameters pH, pO2, pCO2, cK+, cNa+, cCa2+, cCl , cGlu, cLac, cCrea, ctBil, and co-oximetry parameters (ctHb, sO2, and the hemoglobin fractions FO2Hb, FCOHb, FMetHb, FHHb and FHbF)…
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1642-2020·2020-04-15
Biomet Recalls StageOne Hip Cement Spacer Molds Due to Cleaning Concerns
Biomet is recalling StageOne Hip Cement Spacer Molds because the cleaning process may have been insufficient or inadequately monitored.
Product
BIOMET StageOne Hip Cement Spacer Mold with Insert, 64 MM, Silicone, Sterile, Item 431185.
Category
Medical Device
Distribution
49 states
HighFDA (Devices)·Z-1688-2020·2020-04-15
Abbott Recalls Hemoglobin A1c Calibrators Due to Potential Test Bias
Abbott Laboratories is recalling 198 kits of Hemoglobin A1c Calibrators because a manufacturing defect may cause biased patient test results outside a specific concentration range.
Product
"HEMOGLOBIN A1c CALIBRATORS *** REF 4P52-01 *** 307261/R03 *** S4P5X0 *** FOR USE WITH ARCHITECT" - Product Usage: use in the calibration of the Hemoglobin A1c assay.
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1683-2020·2020-04-15
Firefly Child Seats Recalled Due to Broken Latches
James Leckey Design Ltd is recalling Firefly child seats because of reports of broken latches.
Product
Firefly Floorsitter, Firefly Splashy Bathseat, Firefly GoTo Seat - Product Usage: The Splashy Bath-Seat is a Portable bath seat for children aged 1-8, The GoTo Seat is a light-weight, portable, postural support seat for kids, aged between 1 and 8 with disabilities.
Category
Consumer Product
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1641-2020·2020-04-15
Biomet Hip Cement Spacer Mold Recalled for Cleaning Process Concerns
Biomet is recalling StageOne Hip Cement Spacer Molds due to potentially insufficient cleaning processes or inadequate monitoring of cleaning parameters.
Product
BIOMET StageOne Hip Cement Spacer Mold with Insert, 60 MM, Silicone, Sterile, Item 431184.
Category
Medical Device
Distribution
49 states
HighFDA (Devices)·Z-1682-2020·2020-04-15
Change Healthcare Cardiology ECG Software Recalled for Heart Rate Estimation Errors
Change Healthcare Canada Company is recalling McKesson and Change Healthcare Cardiology ECG Management software due to potential inaccurate heart rate estimation in Sequential ECG format.
Product
McKesson Cardiology ECG Management, Change Healthcare Cardiology ECG Management
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1643-2020·2020-04-15
Biomet Recalls Hip Stem Cement Spacer Molds Due to Cleaning Concerns
Biomet is recalling 230,001 units of StageOne Select Hip Stem Cement Spacer Molds due to potentially insufficient cleaning processes.
Product
BIOMET StageOne Select, Hip Stem Cement Spacer Mold w/Reinforcement Cement, 9 X 125 MM, Silicone, Sterile, Item 431190.
Category
Medical Device
Distribution
49 states
HighFDA (Devices)·Z-1689-2020·2020-04-15
Bard Jamshidi Bone Marrow Biopsy Needle Recalled for Sterility Compromise
Bard Peripheral Vascular Inc is recalling Jamshidi Bone Marrow Biopsy/Aspiration Needles because packaging pouches may not be sealed properly, compromising sterility.
Product
Jamshidi Bone Marrow Biopsy/Aspiration Needle, with Luer Lock Adapter 11GX4 ASP, Sterile - Product Code: DJ4011X - Product Usage: The device is comprised of an outer cannula with a handle and an inner stylet. Its intended use is for the posterior iliac crest biopsy technique.
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1638-2020·2020-04-15
Biomet Recalls Hip Cement Spacer Molds Due to Cleaning Process Concerns
Biomet, Inc. is recalling 230,001 units of StageOne Hip Cement Spacer Molds because of potentially insufficient cleaning processes or inadequate monitoring of cleaning parameters.
Product
BIOMET StageOne Hip Cement Spacer Mold with Insert, 48 MM, Silicone, Sterile, Item 431181.
Category
Medical Device
Distribution
49 states
HighFDA (Devices)·Z-1660-2020·2020-04-15
Biomet Shoulder Cement Spacer Mold Recalled for Cleaning Process Concerns
Biomet, Inc. is recalling 230,001 units of StageOne Shoulder Cement Spacer Molds due to potentially insufficient cleaning processes or inadequate monitoring of cleaning parameters.
Product
BIOMET StageOne, Shoulder Cement Spacer Mold 12 MM, 54 X 21 X 64 MM, Silicone, Sterile, Item 431412.
Category
Medical Device
Distribution
49 states
HighFDA (Devices)·Z-1647-2020·2020-04-15
Biomet Hip Stem Cement Spacer Mold Recalled for Cleaning Process Concerns
Biomet is recalling 230,001 hip stem cement spacer molds due to potentially insufficient cleaning processes or inadequate monitoring of cleaning parameters.
Product
BIOMET StageOne Select, Hip Stem Cement Spacer Mold w/Reinforcement Cement, 17 X 165 MM, Silicone, Sterile, Item 431194.
Category
Medical Device
Distribution
49 states
HighFDA (Devices)·Z-1654-2020·2020-04-15
Biomet Recalls Hip Cement Spacer Molds Due to Cleaning Process Concerns
Biomet, Inc. is recalling 230,001 units of StageOne Hip Cement Spacer Molds due to potentially insufficient cleaning processes or inadequate monitoring of cleaning parameters.
Product
BIOMET StageOne, Hip Cement Spacer Mold w/Reinforcement, 9 X 125 MM, 51 MM, Silicone, Sterile, Item 431209.
Category
Medical Device
Distribution
49 states
HighFDA (Devices)·Z-1674-2020·2020-04-15
Beckman Coulter MicroScan PROMPT Inoculation System-D Recalled for Incorrect Wands
Beckman Coulter is recalling 3,472 units of the MicroScan PROMPT Inoculation System-D because they contain incorrect prompt wands, which may cause inaccurate antimicrobial susceptibility test results.
Product
Beckman Coulter MicroScan PROMPT Inoculation System-D, Catalog Number B1026-10D, UDI: 15099590659561 - Product Usage: The Prompt Inoculation System-D is used to standardize inocula for microdilution antimicrobial susceptibility test.
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1671-2020·2020-04-15
Abbott ARCHITECT C System Mixer Recall Due to Blade Separation Risk
Abbott is recalling ARCHITECT C System Mixers because the blade may separate from the mixer due to screw and nut failure, leading to inadequate mixing of samples and reagents.
Product
ARCHITECT C System Mixer - Product Usage: The ARCHITECT Clinical Chemistry System is designed to perform automated chemistry tests, utilizing photometry and potentiometric technology. The mixer is a component and it is used on all ARCHITECT Clinical Chemistry systems to mix the…
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-1653-2020·2020-04-15
Biomet Recalls Hip Cement Spacer Molds Due to Cleaning Process Concerns
Biomet, Inc. is recalling 230,001 units of BIOMET StageOne Hip Cement Spacer Molds due to potentially insufficient cleaning processes or inadequate monitoring of cleaning parameters.
Product
BIOMET StageOne, Hip Cement Spacer Mold w/Reinforcement, 9 X 125 MM, 43 MM, Silicone, Sterile, Item 431207.
Category
Medical Device
Distribution
49 states
ModerateFDA (Devices)·Z-1669-2020·2020-04-15
Biomet Recalls Knee Tibial Cement Spacer Molds Due to Cleaning Concerns
Biomet is recalling 230,001 units of StageOne Knee Tibial Cement Spacer Molds because of potentially insufficient cleaning processes or inadequate monitoring of cleaning parameters.
Product
BIOMET StageOne Knee Tibial Cement Spacer Mold, 80 MM, Silicone, Sterile, Item 433180.
Category
Medical Device
Distribution
49 states
ModerateFDA (Devices)·Z-1649-2020·2020-04-15
Biomet Hip Stem Cement Spacer Mold Recalled for Cleaning Process Concerns
Biomet is recalling hip stem cement spacer molds due to potentially insufficient cleaning processes or inadequate monitoring of cleaning parameters.
Product
BIOMET StageOne Select, Hip Stem Cement Spacer Mold w/Reinforcement Cement, 11 X 200 MM, Silicone, Sterile, Item 431196.
Category
Medical Device
Distribution
49 states
ModerateFDA (Devices)·Z-1663-2020·2020-04-15
Biomet Recalls Knee Spacer Molds Due to Insufficient Cleaning Process
Biomet, Inc. is recalling 230,001 units of StageOne Knee Femoral Cement Spacer Molds due to potentially insufficient cleaning or inadequate process monitoring.
Product
BIOMET StageOne Knee Femoral Cement Spacer Mold, 65 MM, Silicone, Sterile, Item 432165.
Category
Medical Device
Distribution
49 states
ModerateFDA (Devices)·Z-1655-2020·2020-04-15
Biomet Recalls Hip Cement Spacer Molds Due to Cleaning Process Concerns
Biomet, Inc. is recalling StageOne Hip Cement Spacer Molds because of a potentially insufficient cleaning process or inadequate monitoring of cleaning parameters.
Product
BIOMET StageOne, Hip Cement Spacer Mold w/Reinforcement, 13 X 145 MM, 57 MM, Silicone, Sterile, Item 431213.
Category
Medical Device
Distribution
49 states