Class IIOngoingZ-1818-2026
Integra LifeSciences Corp. (NeuroSciences) recalls Cytal Wound Matrix 2-Layer 10x15 cm. Product ID: WSM1015.
Increased rate of out-of-specification endotoxin results.
Integra LifeSciences C…NJApr 22, 2026
Recalls: Under Investigation by firm
Drawn from openFDA device enforcement reports. Filter by severity, status, state, year, or manufacturer.
Showing 217–228 of 1,121 recalls
Class IIOngoingZ-1817-2026
Integra LifeSciences Corp. (NeuroSciences) recalls Cytal Wound Matrix 2-Layer 7x10 cm. Product ID: WSM0710.
Increased rate of out-of-specification endotoxin results.
Integra LifeSciences C…NJApr 22, 2026
Class IIOngoingZ-1816-2026
Integra LifeSciences Corp. (NeuroSciences) recalls Cytal Wound Matrix 2-Layer 5x5 cm. Product ID: WSM0505.
Increased rate of out-of-specification endotoxin results.
Integra LifeSciences C…NJApr 22, 2026
Class IIOngoingZ-1810-2026
Linkbio Corp. recalls LinkBio CORE Workstation
The CORE Workstation may display an incorrect "Planning Date " when viewing cases on the "Start Case" menu screen.
Linkbio Corp.NJApr 22, 2026
Class IIOngoingZ-1806-2026
Remel, Inc recalls Yeastone Broth
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 Quality Control test result.
Remel, IncKSApr 22, 2026
Class IIOngoingZ-1795-2026
Brahms GmbH recalls B.R.A.H.M.S PlGF Plus KRYPTOR
Customers have observed quality control values out of range at the lowest quality control level (QC Level 1) for the PIGF assay which require troubleshooting steps to resolve.…
Brahms GmbHApr 15, 2026
Class IIOngoingZ-1794-2026
Beckman Coulter, Inc. recalls MicroScan Neg Multidrug Resistant MIC 1 REF C32368 UDI-DI code: 15099590720568 Inte…
Due to manufacturing issue (incorrectly processing) with in vitro multidrug resistant test.
Beckman Coulter, Inc.CAApr 15, 2026
Class IIOngoingZ-1773-2026
XTANT Medical Holdings, Inc recalls XTANT MEDICAL Xpress Pedicle Screw System Dual Lead 6.5 x 50 mm
Units from one lot were mislabeled with an incorrect part number, identifying the device as a shorter screw length than it physically is.
XTANT Medical Holdings…MTApr 15, 2026
Class IOngoingZ-1730-2026
Medline Industries, LP recalls Medline medical convenience kits
Medline Industries, LP has identified through post-market surveillance a potential risk of the syringe rotating adaptor unwinding during use, which may result in a loose connection and/or full disconnection between the s…
Medline Industries, LPILApr 15, 2026
Class IOngoingZ-1729-2026
Medline Industries, LP recalls Medline medical convenience kits
Medline Industries, LP has identified through post-market surveillance a potential risk of the syringe rotating adaptor unwinding during use, which may result in a loose connection and/or full disconnection between the s…
Medline Industries, LPILApr 15, 2026
Class IOngoingZ-1728-2026
Medline Industries, LP recalls Medline medical convenience kits
Medline Industries, LP has identified through post-market surveillance a potential risk of the syringe rotating adaptor unwinding during use, which may result in a loose connection and/or full disconnection between the s…
Medline Industries, LPILApr 15, 2026
Class IOngoingZ-1727-2026
Medline Industries, LP recalls Medline medical convenience kits
Medline Industries, LP has identified through post-market surveillance a potential risk of the syringe rotating adaptor unwinding during use, which may result in a loose connection and/or full disconnection between the s…
Medline Industries, LPILApr 15, 2026