DrugOct 25, 2023
Doxil recall — FDA D-0048-2024
CGMP Deviations: Product was exposed to temperatures exceeding the labeled storage conditions during transportation were released by mistake.
Class IIFDA: TerminatedBaxter Healthcare Corporation
Latest records
Latest recalls — page 493
The newest recall records with useful source details are listed here.
VehicleOct 19, 2023
Honda rack and pinion recall — NHTSA campaign 23V704000
Honda (American Honda Motor Co.) is recalling certain 2022-2024 Civic 4-door and Civic 5-door vehicles that received a replacement power steering rack as part of a service repair. The…
rack and pinionHonda (American Honda Motor Co.)
Medical DeviceOct 18, 2023
Cardinal Health 200 Procedure packs: (1) Presource PBDS Cat recall — FDA Z-0086-2024
Packs contain recalled components (equipment drapes, table cover, and surgical room turnover (SRT) kits).
Class IIFDA: OngoingCardinal Health 200, LLC
Medical DeviceOct 18, 2023
CareFusion 303 BD Pyxis CII Safe ES, REF: 1116-00 recall — FDA Z-0093-2024
When global edit is used to update multiple formulary properties simultaneously, the following properties: 1) Require Lot Number on Recall, 2) Access Destruction Bin (Witness), 3) Add to…
Class IIFDA: OngoingCareFusion 303, Inc.
Medical DeviceOct 18, 2023
Smiths Medical ASD Medfusion PLUNGER FLOAT PLATE, Component Number G6000069, used on recall — FDA Z-0080-2024
A force sensor in the occlusion detector may drift out of calibration leading to increased occlusion detection times, false occlusion alarms, or a System Failure Alarm. If the force sensor…
Class IIFDA: OngoingSmiths Medical ASD Inc.
Medical DeviceOct 18, 2023
Cardinal Health 200 Procedure packs: (1) Presource Portacath Pack, Cat recall — FDA Z-0088-2024
Packs contain recalled components (equipment drapes, table cover, and surgical room turnover (SRT) kits).
Class IIFDA: OngoingCardinal Health 200, LLC
Medical DeviceOct 18, 2023
Cardinal Health 200 Procedure packs: (1) Presource PBDS Cat recall — FDA Z-0089-2024
Packs contain recalled components (equipment drapes, table cover, and surgical room turnover (SRT) kits).
Class IIFDA: OngoingCardinal Health 200, LLC
Medical DeviceOct 18, 2023
Smiths Medical ASD Medfusion ASSEMBLY PLUNGER CASE LEFT 1/EA, Component Number G6001587 recall — FDA Z-0081-2024
A force sensor in the occlusion detector may drift out of calibration leading to increased occlusion detection times, false occlusion alarms, or a System Failure Alarm. If the force sensor…
Class IIFDA: OngoingSmiths Medical ASD Inc.
Medical DeviceOct 18, 2023
Olympus Corporation of the Americas THUNDERBEAT, 5MM, 45CM, Front-actuated Grip Type S recall — FDA Z-0109-2024
Thunderbeats blue seal button may remain in the engaged position after the button is released and not immediately return to a neutral position may result in prolonged surgery
Class IIFDA: OngoingOlympus Corporation of the Americas
Medical DeviceOct 18, 2023
Cardinal Health 200 Procedure packs: (1) Presource PBDS, Cat recall — FDA Z-0084-2024
Packs contain recalled components (equipment drapes, table cover, and surgical room turnover (SRT) kits).
Class IIFDA: OngoingCardinal Health 200, LLC
Medical DeviceOct 18, 2023
Ansell Healthcare Products GAMMEX NON-LATEX PI GREEN Surgical gloves, REF: 20685255 through recall — FDA Z-0096-2024
Some surgical glove sterile pouches were not completely sealed.
Class IIFDA: OngoingAnsell Healthcare Products LLC
Medical DeviceOct 18, 2023
TECHNO-PATH MANUFACTURING Multichem IA Plus, Part Codes: a) 08P86-10, b) 08P86-19 recall — FDA Z-0105-2024
Technopath Manufacturing Ltd. has identified an issue with the glass vial commodity used to fill the Multichem S Plus Level 1, Multichem S Plus Level 2, Multichem S Plus Level 3, Multichem…
Class IIFDA: OngoingTECHNO-PATH MANUFACTURING LTD.
Medical DeviceOct 18, 2023
Encore Medical EMPOWR 3D Knee Tibial Insert, 5R, 10MM, VE, REF: 342-10-705 recall — FDA Z-0102-2024
Knee insert and acetabular system parts were swapped within inner pack prior to the product being sealed within the tray, which could result in surgeons not having the correct product for…
Class IIFDA: OngoingEncore Medical, LP
Medical DeviceOct 18, 2023
Encore Medical EMPOWR Acetabular System, Liner, 10 Hooded, HXe+, 40H, REF: 942-01-40H recall — FDA Z-0103-2024
Knee insert and acetabular system parts were swapped within inner pack prior to the product being sealed within the tray, which could result in surgeons not having the correct product for…
Class IIFDA: OngoingEncore Medical, LP
Medical DeviceOct 18, 2023
Cardinal Health 200 Presource Fistulogram Pack, Cat recall — FDA Z-0092-2024
Packs contain recalled components (equipment drapes, table cover, and surgical room turnover (SRT) kits).
Class IIFDA: OngoingCardinal Health 200, LLC
Medical DeviceOct 18, 2023
Cardinal Health 200 Procedure packs: (1) Presource PBDS, Cat recall — FDA Z-0087-2024
Packs contain recalled components (equipment drapes, table cover, and surgical room turnover (SRT) kits).
Class IIFDA: OngoingCardinal Health 200, LLC
Medical DeviceOct 18, 2023
Flower Orthopedics Coventus Flower Orthopedics Flex-Thread TM 3.2mm Cannulated Reamer-used recall — FDA Z-0074-2024
Device is breaking while in use, potential for patients to require a revision surgery.
Class IIFDA: OngoingFlower Orthopedics Corporation
Medical DeviceOct 18, 2023
Beckman Coulter Access Thyroglobulin Calibrators recall — FDA Z-0100-2024
It has been determined through an internal investigation that the alternate Access Thyroglobulin calibrator cards for use with the Thyg reagent packs distributed in April 2023 will cause a…
Class IIFDA: OngoingBeckman Coulter, Inc.
Medical DeviceOct 18, 2023
Advance-Esthetic MED-810A Zemits NDPrime Laser products recall — FDA Z-0095-2024
Advance-Esthetic LLC failed to comply with the applicable standards regarding Electronic Product Radiation Control (EPRC) regulations associated with the laser product performance standards…
Class IIFDA: OngoingAdvance-Esthetic LLC
Medical DeviceOct 18, 2023
Smiths Medical ASD Medfusion Syringe Pump, Model 3500VX-500, v3, v4, v5, and v6 recall — FDA Z-0077-2024
A force sensor in the occlusion detector may drift out of calibration leading to increased occlusion detection times, false occlusion alarms, or a System Failure Alarm. If the force sensor…
Class IIFDA: OngoingSmiths Medical ASD Inc.
Medical DeviceOct 18, 2023
Beckman Coulter DxI 9000 Access Immunoassay Analyzer, REF C11137, Sofware Versions 1.15 and recall — FDA Z-0107-2024
The firm has investigated and confirmed that when DxI 9000 is connected to Laboratory Information System (LIS, host), the sample barcode presented may be ignored and replaced with a sample…
Class IIFDA: OngoingBeckman Coulter, Inc.
Medical DeviceOct 18, 2023
TECHNO-PATH MANUFACTURING Multichem S Plus, Part Codes: a) 08P88-10, b) 08P88-11, c) recall — FDA Z-0104-2024
Technopath Manufacturing Ltd. has identified an issue with the glass vial commodity used to fill the Multichem S Plus Level 1, Multichem S Plus Level 2, Multichem S Plus Level 3, Multichem…
Class IIFDA: OngoingTECHNO-PATH MANUFACTURING LTD.
Medical DeviceOct 18, 2023
Cardinal Health 200 Procedure packs: (1) Presource PBDS Cat recall — FDA Z-0091-2024
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Class IIFDA: OngoingCardinal Health 200, LLC
Medical DeviceOct 18, 2023
Cardinal Health 200 Procedure packs: (1) Presource Pain Tray, Catalog SBAHFPTAS2, Advanced recall — FDA Z-0083-2024
Packs contain recalled components (equipment drapes, table cover, and surgical room turnover (SRT) kits).
Class IIFDA: OngoingCardinal Health 200, LLC
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Recent recall archives
Browse recent months with enough recall history for useful comparison.
September 2026364 records · 4 categoriesAugust 2026302 records · 4 categoriesJuly 2026370 records · 4 categoriesJune 2026376 records · 4 categoriesMay 2026340 records · 4 categoriesApril 2026415 records · 4 categoriesMarch 2026190 records · 4 categoriesFebruary 2026331 records · 4 categoriesJanuary 2026212 records · 4 categoriesDecember 2025389 records · 4 categoriesNovember 2025326 records · 4 categoriesOctober 2025455 records · 4 categories