DrugApr 29, 2026
Claravis recall — FDA D-0521-2026
Failed Impurities/Degradation Specifications: Out of specification for specific impurity Tretinoin
Class IIFDA: OngoingTeva Pharmaceuticals USA, Inc
Monthly breakdown
2026 recalls by month
Select a month to review the recall records reported during that period.
August 2026145 records · 4 categoriesJuly 2026369 records · 4 categoriesJune 2026372 records · 4 categoriesMay 2026330 records · 4 categoriesApril 2026407 records · 4 categoriesMarch 2026179 records · 4 categoriesFebruary 2026326 records · 4 categoriesJanuary 2026210 records · 4 categories
2026 recalls — page 55
Records are ordered by the best available source date.
DrugApr 29, 2026
MONSELS SOLUTION Premier, Monsel's, Ferric Subsulfate Solution, 8 mL bottles recall — FDA D-0490-2026
Labeling: Incorrect or Missing Lot and/or Exp Date:The expiration date has an extra digit and is printed as 2709114 instead of the correct 270914 (2027-09-14). It is important to note that…
Class IIIFDA: OngoingPremier Dental Products Co
DrugApr 29, 2026
OMEGA-3-ACID ETHYL ESTERS Omega-3-Acid, Ethyl Esters, Capsules, USP, 1 gram, 50 capsules recall — FDA D-0493-2026
Failed Capsule Specifications: Out of specification results obtained during routine stability testing for Loss on Drying of Capsule Shells.
Class IIFDA: OngoingThe Harvard Drug Group LLC
Medical DeviceApr 22, 2026
B Braun Medical B. Braun Hemodialysis Bloodlines, STREAMLINE BLOODLINE SET FOR DIALOG recall — FDA Z-1799-2026
Potential for the accumulation of small air bubbles in the arterial line due to adherence of blood gases to the tubing under negative pressure.
Class IFDA: OngoingB Braun Medical Inc
Medical DeviceApr 22, 2026
B Braun Medical B. Braun Hemodialysis Bloodlines, LOW VOL, NO CHAMBER 2.6MM PUMP SEGMENT recall — FDA Z-1802-2026
Potential for the accumulation of small air bubbles in the arterial line due to adherence of blood gases to the tubing under negative pressure.
Class IFDA: OngoingB Braun Medical Inc
Medical DeviceApr 22, 2026
B Braun Medical B Braun Hemodialysis Bloodlines, LOW VOL, NO CHAMBER 4.8MM PUMP SEGMENT recall — FDA Z-1803-2026
Potential for the accumulation of small air bubbles in the arterial line due to adherence of blood gases to the tubing under negative pressure.
Class IFDA: OngoingB Braun Medical Inc
Medical DeviceApr 22, 2026
LinkBio CORE Workstation, a component of the CORE Shoulder System recall — FDA Z-1810-2026
The CORE Workstation may display an incorrect "Planning Date " when viewing cases on the "Start Case" menu screen.
Class IIFDA: OngoingLinkbio Corp.
Medical DeviceApr 22, 2026
B Braun Medical B. Braun Hemodialysis Bloodlines, STREAMLINE FRESENIUS FOR DAVITA recall — FDA Z-1800-2026
Potential for the accumulation of small air bubbles in the arterial line due to adherence of blood gases to the tubing under negative pressure.
Class IFDA: OngoingB Braun Medical Inc
Medical DeviceApr 22, 2026
B Braun Medical B. Braun Hemodialysis Bloodlines, STREAMLINE BLOODLINE SET FOR DIALOG DR recall — FDA Z-1798-2026
Potential for the accumulation of small air bubbles in the arterial line due to adherence of blood gases to the tubing under negative pressure.
Class IFDA: OngoingB Braun Medical Inc
Medical DeviceApr 22, 2026
Siemens Medical Solutions USA ARTIS Pheno VE30A and VE40A, Model 10849000 recall — FDA Z-1814-2026
During 3D acquisitions, lighter and darker patient images may be captured, which may result in less accurate 3D reconstruction. The variation of brightness is a result of a constant…
Class IIFDA: OngoingSiemens Medical Solutions USA, Inc
Medical DeviceApr 22, 2026
Philips Spectral CT on Rails recall — FDA Z-1825-2026
Philips has identified three software issues: 1. During a continuous CT (CCT) scan, there is the potential that the Gantry could remain at the current scan position after pressing Go. 2.…
Class IIFDA: OngoingPHILIPS MEDICAL SYSTEMS
Medical DeviceApr 22, 2026
B Braun Medical B. Barun Hemodialysis Bloodlines, StreamLine Bloodline Long Version, FMC recall — FDA Z-1801-2026
Potential for the accumulation of small air bubbles in the arterial line due to adherence of blood gases to the tubing under negative pressure.
Class IFDA: OngoingB Braun Medical Inc
Medical DeviceApr 22, 2026
ELEGANCE 1 LEVEL CERVICAL PLATE, ELEGANCE 2 LEVEL CERVICAL PLATE, ELEGANCE 3 LEVEL CERVICAL recall — FDA Z-1821-2026
Due to a quality issue regarding the presence of burr on the finished cervical plate product.
Class IIFDA: OngoingClariance-SAS
Medical DeviceApr 22, 2026
Beta Bionics iLet Ace Pump Kit REF: BB1001 iLet Dosing Decision Software recall — FDA Z-1809-2026
it was found that in versions 1.3.7, 1.4.2, and 1.4.3, the Lock Screen and Limited Access Passcode Screen on the iLet graphical user interface (GUI) include certain icons displayed in the…
Class IIFDA: OngoingBeta Bionics, Inc.
Medical DeviceApr 22, 2026
Philips AneurysmFlow recall — FDA Z-1805-2026
Potential safety issue involving the Mean Aneurysm Flow Amplitude (MAFA) ratio of AneurysmFlow (Interventional Tool). Philips has determined that the MAFA ratio does not provide reliable…
Class IIFDA: OngoingPHILIPS MEDICAL SYSTEMS NEDERLAND B.V.
Medical DeviceApr 22, 2026
CELLEX Photopheresis Kit recall — FDA Z-1822-2026
Increased difficulty in installing the centrifuge bowl onto the centrifuge bowl holder. Improper installation may cause the centrifuge bowl to dislodge, resulting in a broken bowl during…
Class IIFDA: OngoingTHERAKOS DEVELOPMENT LIMITED
Medical DeviceApr 22, 2026
Wilson-Cook Medical Instinct Plus Endoscopic Clipping Device REF: G58010 Rx Only, Sterile EO recall — FDA Z-1812-2026
Due to increased in complaints their is the potential for endoscopic clipping device to malfunction.
Class IIFDA: OngoingWilson-Cook Medical Inc.
Medical DeviceApr 22, 2026
Gentuity HF-OCT Imaging System Model G10-01 recall — FDA Z-1823-2026
The potential for repeated frames during HF-OCT pullback when using the Gentuity HF-OCT Console (software version 21.11 to 23.3.13) with the Vis-Rx and Vis-Rx Prime catheters. This…
Class IIFDA: OngoingGentuity, LLC
Medical DeviceApr 22, 2026
Remel Yeastone Broth, 11ML, 10/BOX YY3462 recall — FDA Z-1806-2026
Products may report incorrect AST results during quality control. Health consequences may include delayed response or the need to change to another antifungal agent if laboratory ignores…
Class IIFDA: OngoingRemel, Inc
Medical DeviceApr 22, 2026
Insulet Omnipod 5 Pods recall — FDA Z-1797-2026
Due to a manufacturing defect, certain Omnipod 5 Pods from 49 lots have an internal soft cannula tear that results in insulin leaking into the Pod instead of being delivered to the user…
Class IFDA: OngoingInsulet Corporation
Medical DeviceApr 22, 2026
ARJOHUNTLEIGH POLSKA Sp. z.o.o Arjo Tenor mobile passive patient lift, Model Numbers KHA1000 recall — FDA Z-1811-2026
An internal component of the actuators in a certain production batch may not meet the required mechanical strength. This could result, in the worst case scenario, in a sudden loss of the…
Class IIFDA: OngoingARJOHUNTLEIGH POLSKA Sp. z.o.o.
VehicleApr 22, 2026
RAV 4 critical fasteners recall — NHTSA campaign 26V256000
Toyota Motor Engineering & Manufacturing (Toyota) is recalling certain 2025 RAV 4 vehicles. The front seat brackets for the seat rails may be welded improperly.
critical fastenersToyota Motor Engineering & Manufacturing
FoodApr 22, 2026
PURE PALM C/O DVD Label is predominantly green with white lettering in a clear recall — FDA H-0681-2026
mislabeled Coconut Date Bites. (product is coconut covered, label is for regular date bites)
Class IIFDA: TerminatedPURE PALM C/O DVD
FoodApr 22, 2026
Bee Well Honey Farm & Supply Raw & Unfiltered Bee Well Wildflower Honey NET wT recall — FDA H-0664-2026
High sugar content. The firm was notified by the FDA that sample results were positive for a high C4 sugar content.
Class IIIFDA: TerminatedBee Well Honey Farm & Supply Inc.
About the 2026 recall archive
This archive groups records by their reported or recall date. It does not imply that every recall was initiated, announced and resolved during the same calendar year. Open the individual record for the exact dates and source details supplied by FDA or NHTSA.