State

Oklahoma product recalls

73,824 recalls have nationwide distribution and so reach Oklahoma. 5,823 additional recalls listed Oklahoma specifically in their distribution scope.

What the numbers show

Total: 5,823
Critical: 1,040
Severe: 1,494
Most recent: 2026-11-04

Of the 5,823 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 1,494 (26%) are Severe.

Which agencies issued them

These figures cover only the 5,823 recalls whose distribution notice names Oklahoma specifically. The 73,824 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.

52451–52475 of 79647

HighFDA (Devices)·Z-1844-2016·2016-06-08
Skytron EZ Slide Operating Table Recalled for Potential Slide Cap Detachment
Skytron is recalling 458 EZ Slide Operating Tables because incorrectly manufactured parts may cause the slide cap to detach, risking injury to patients or staff.
Product
EZ Slide Battery/line powered hydraulic table with removable leg section and 21 top slide General Purpose Surgical Table Skytron EZ Slide Operating Table General Purpose Surgical Table
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1861-2016·2016-06-08
Fujifilm ED-250XL5 Endoscope Manual Correction for Infection Control
Fujifilm Medical Systems is correcting the ED-250XL5 endoscope operations manual to address reports of multi-drug resistant bacteria on endoscopes used for ERCP procedures.
Product
Endoscope ED-250XL5 Operations Manual: Cleaning, Disinfection
Category
Medical Device
Distribution
Distributed nationwide
HighCPSC·16190·2016-06-08
Kwik Tek Recalls Hammerhead Sleds Due to Crash Hazard
Kwik Tek is recalling Hammerhead sleds because the front handle bar assembly can break, posing a crash hazard. No injuries have been reported.
Product
Sleds
Category
Consumer Product
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1850-2016·2016-06-08
Kerlix X-Ray Detectable Laparotomy Sponges Recalled for Sterility Breach
The FDA is recalling Kerlix X-Ray Detectable Laparotomy Sponges due to compromised sterility from a barrier breach.
Product
Kerlix X-Ray Detectable Laparotomy Sponges, Tray Pack, 17" x 26" (43.2 cm x 66 cm) Item Number: 4031
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Food)·F-1419-2016·2016-06-08
Buddy Fruits Recalls Lemon Fruit Tartlets Due to Undeclared Milk
Ouhlala Gourmet LLC is recalling lemon fruit tartlets because the finished product contains undeclared milk. The recall covers 9,159 cases distributed nationwide and internationally.
Product
Fruit Tartlets, lemon flavor, 9 - 0.53oz (15 g) tartlets - Net Wt. 4.8 oz (135 g). Manufactured in France. Distributed by Ouhlala Gourmet Corp. dba Buddy Fruits, Coral Gables, FL
Category
Food
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1878-2016·2016-06-08
Natus Medical Recalls Replacement HEPA Filters for Sterile-Driers
Natus Medical is recalling 21 replacement HEPA filters for Sterile-Driers because improperly cured sealant may emit toxic gas or drip, contaminating the device.
Product
Replacement HEPA filter for Natus Sterile-Drier Model 43 and Model 44. Filter Catalogue Part Number: 54343, 54344, and 100105-01.
Category
Medical Device
Distribution
18 states
HighNHTSA·16E053000·2016-06-08
Thule Recalls Sprint Bicycle Carriers Due to Fork Clamping Defect
Thule is recalling certain Sprint bicycle carriers because the fork clamping mechanism may not secure the bike, allowing it to detach from the vehicle.
Product
EQUIPMENT:MECHANICAL:CARRIER/RACK recall
Category
Consumer Product
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1864-2016·2016-06-08
Fujifilm ED-450XL5 Endoscope Manual Correction for Infection Control
Fujifilm Medical Systems is correcting the operation manual for the ED-450XL5 endoscope to address publicized reports of multi-drug resistant bacteria on endoscopes used for ERCP procedures.
Product
Endoscope ED-450XL5 Operation Manual: Cleaning, Disinfection and Storage
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-1873-2016·2016-06-08
Philips Ingenuity Core CT Systems Recalled for Drive Mapping Issue
Philips is recalling 300 Ingenuity Core CT systems because they may fail to map the Varian drive after a user logs out and back in.
Product
Ingenuity Core Computed Tomography X-ray Systems, Product Usage: Intended to produce cross-sectional images of the body by computer reconstruction of X-ray transmission data taken at different angles and planes.
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-1845-2016·2016-06-08
Olympus Recalls Duodenoscopes for New Reprocessing Instructions
Olympus Corporation of the Americas is recalling TJF-160F and TJF-160VF duodenoscopes to provide new reprocessing instructions and a cleaning brush.
Product
EVIS EXERA Duodenovideoscope Olympus TJF Type 160F/VF used with an Olympus video system center, light source, documentation equipment monitors, Endo Therapy accessories and other ancillary equipment for endoscopy and endoscopic surgery within the duodenum.
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-1872-2016·2016-06-08
Philips Brilliance 64 CT Systems Recalled for Software Mapping Error
Philips Medical Systems is recalling 158 Brilliance 64 CT systems because the software may fail to map the Varian drive after a user logs out and back in.
Product
Brilliance 64 Computed Tomography X-ray Systems Product Usage: Intended to produce cross-sectional images of the body by computer reconstruction of X-ray transmission data taken at different angles and planes.
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-1901-2016·2016-06-08
Exactech Recalls Two Novation Ceramic Hip Acetabular Cups
Exactech is recalling two Novation Ceramic AHS Cluster-Hole Shell acetabular cups because they were packaged before regulatory approval.
Product
Novation Ceramic AHS Cluster-Hole Shell, Plasma Coated, 56mm, O.D. (Acetabular Cup), Catalog Number 140-01-56; For use in primary total hip arthroplasty.
Category
Medical Device
Distribution
9 states
ModerateFDA (Drugs)·D-0950-2016·2016-06-08
Taro Recalls Subpotent Topicort Cream Tubes in Multiple States
Taro Pharmaceuticals is recalling 62,800 tubes of Topicort cream because the medication contained less active ingredient than labeled.
Product
¿Topicort (desoximetasone) Cream USP, 0.05%, Packaged in 5 g Tubes, Professional Sample Only, Rx Only. Mfd. by: Taro Pharmaceuticals Inc., Brampton, Ontario, Canada L6T 1C1, Dist. by: TaroPharma a division of Taro Pharmaceuticals U.S.A., Inc., Hawthorne, NY 10532. NDC…
Category
Drug
Distribution
9 states
ModerateFDA (Devices)·Z-1904-2016·2016-06-08
Exactech Recalls One Novation Femoral Stem Device for Premature Packaging
Exactech is recalling one Novation femoral stem device because it was packaged before the required site-change approval was granted.
Product
Novation Press-Fit Tapered, Standard Offset, HA Coated, 12/14 Taper, Femoral Stem; Catalog Number 160-10-16; For use in primary total hip arthroplasty.
Category
Medical Device
Distribution
9 states
ModerateFDA (Devices)·Z-1865-2016·2016-06-08
Abbott ARCHITECT Estradiol Kit Recalled for Fulvestrant Interference
Abbott Laboratories is recalling ARCHITECT Estradiol Kits because interaction with the drug Fulvestrant causes falsely elevated estradiol results.
Product
The ARCHITECT Estradiol Kit Intended to measure estradiol, an estrogenic steroid, in plasma.
Category
Medical Device
Distribution
42 states
ModerateFDA (Devices)·Z-1840-2016·2016-06-08
Baxter Recalls COSEAL Surgical Sealant Kits Due to Dissolution Issues
Baxter Healthcare is recalling 6,128 COSEAL Surgical Sealant Kits because the PEG component may not fully dissolve, affecting hydrogel consistency.
Product
COSEAL Surgical Sealant Kit, 8 mL, Product Code: 934072; For use in vascular reconstructions to achieve adjunctive hemostasis by mechanically sealing areas of leakage.
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-1838-2016·2016-06-08
Baxter Recalls COSEAL Surgical Sealant Kits Due to Dissolution Issues
Baxter Healthcare is recalling 274 units of COSEAL Surgical Sealant Kits because the PEG component may not fully dissolve, affecting hydrogel consistency.
Product
COSEAL Surgical Sealant Kit, 2 mL, Product Code: 934070; For use in vascular reconstructions to achieve adjunctive hemostasis by mechanically sealing areas of leakage.
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-1905-2016·2016-06-08
Exactech Recalls Novation Femoral Stems Due to Premature Packaging
Exactech is recalling nine Novation femoral stems because they were packaged before receiving FDA approval for a site change.
Product
Novation Press-Fit Splined, Standard Offset, HA Coated, 12/14 Taper, Size 11, Femoral Stem; Catalog Number 160-30-11; For use in primary total hip arthroplasty.
Category
Medical Device
Distribution
9 states
ModerateFDA (Devices)·Z-1903-2016·2016-06-08
Exactech Recalls One Novation Femoral Stem for Premature Packaging
Exactech is recalling one Novation femoral stem device because it was packaged before the required FDA site-change approval was granted.
Product
Novation Press-Fit Tapered, Standard Offset, 12/14 Taper, Size 14, Femoral Stem, Catalog Number 160-00-14; For use in primary total hip arthroplasty.
Category
Medical Device
Distribution
9 states
ModerateFDA (Devices)·Z-1843-2016·2016-06-08
Medscience AllergiEnd Skin Test Applicators Recalled for Lack of Clearance
Medscience Inc is recalling AllergiEnd ST-9 skin test applicators and trays because they were marketed without FDA clearance.
Product
AllergiEnd ST-9 Multiple Skin Test Applicator (Item 1000) and AllergiEnd ST-9 Multiple Well Test Tray (Item (1001). Contents: 8 applicators to perform up to 72 skin tests. Perform a multi-site skin test to identify reactions to certain allergens using a non-invasive applicator…
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-1874-2016·2016-06-08
Philips Ingenuity Core 128 CT Systems Recalled for Drive Mapping Issue
Philips Medical Systems is recalling 424 Ingenuity Core 128 CT systems because the system may not map the Varian drive after a user logout and login.
Product
Ingenuity Core 128 Computed Tomography X-ray Systems Product Usage: Intended to produce cross-sectional images of the body by computer reconstruction of X-ray transmission data taken at different angles and planes.
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-1875-2016·2016-06-08
Philips Ingenuity CT Systems Recalled for Drive Mapping Issue
Philips is recalling 215 Ingenuity CT systems because they may fail to map the Varian drive after a user logs out and back in.
Product
Ingenuity Computed Tomography X-ray Systems Product Usage: Intended to produce cross-sectional images of the body by computer reconstruction of X-ray transmission data taken at different angles and planes.
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-1900-2016·2016-06-08
Exactech Recalls Three Ceramic Hip Acetabular Cups Due to Premature Packaging
Exactech is recalling three Novation Ceramic AHS Cluster-Hole Shells because they were packaged before the required site-change approval was granted.
Product
Novation Ceramic AHS Cluster-Hole Shell, Plasma Coated, 54mm, O.D. (Acetabular Cup), Catalog Number 140-01-54; For use in primary total hip arthroplasty.
Category
Medical Device
Distribution
9 states
ModerateFDA (Devices)·Z-1839-2016·2016-06-08
Baxter Recalls COSEAL Surgical Sealant Kits Due to Dissolution Issues
Baxter Healthcare is recalling 6,804 units of COSEAL Surgical Sealant Kits because the PEG component may not fully dissolve, affecting hydrogel consistency.
Product
COSEAL Surgical Sealant Kit, 4 mL, Product Code: 934071; For use in vascular reconstructions to achieve adjunctive hemostasis by mechanically sealing areas of leakage.
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-1902-2016·2016-06-08
Exactech Recalls Four Novation Femoral Stems Due to Premature Packaging
Exactech is recalling four Novation femoral stems because they were packaged before the required site-change approval was granted.
Product
Novation Press-Fit Tapered, Standard Offset, 12/14 Taper, Size 13, Femoral Stem, Catalog Number 160-00-13; For use in primary total hip arthroplasty.
Category
Medical Device
Distribution
9 states