Recalls published in March 2026
Everything the FDA, USDA FSIS, CPSC and NHTSA announced in March 2026, newest first.
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Class II · 7 months ago
Waldemar Link GmbH & Co. KG Endo-Model Replacement Plateau recall: The potential for an implant with a plateau screw where the bushing
The potential for an implant with a plateau screw where the bushing could detach from the screw shaft due to a longitudinal fracture.
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Class II · 7 months ago
Waldemar Link GmbH & Co. KG Endo-Model Replacement Plateau recall: The potential for an implant with a plateau screw where the bushing
The potential for an implant with a plateau screw where the bushing could detach from the screw shaft due to a longitudinal fracture.
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Class II · 7 months ago
Instrumentation Laboratory GEM Premier 5000 PAK recall: Confirmed customer complaints indicating that GEM PAKs (cartridges)
Confirmed customer complaints indicating that GEM PAKs (cartridges) for the GEM Premier 5000 may experience an increased incidence of Process Control…
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Class II · 7 months ago
Boston Scientific Corporation EndoVive Safety PEG Kit recall: Recall of kits which utilized ChloraPrep Triple Swabsticks from BD. Open
Recall of kits which utilized ChloraPrep Triple Swabsticks from BD. Open or compromised seals on the sterile swabstick packaging, which could result…
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Class II · 7 months ago
Altruan GmbH Wondfo Streptococcal A At-Home Self-Test. At-home test for group recall: Product not cleared by the FDA
Product not cleared by the FDA.
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Class II · 7 months ago
Waldemar Link GmbH & Co. KG Endo-Model Replacement Plateau recall: The potential for an implant with a plateau screw where the bushing
The potential for an implant with a plateau screw where the bushing could detach from the screw shaft due to a longitudinal fracture.
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Class III · 7 months ago
Penner Pacific Bathing Spa, Model Numbers 390010-1, 390010-X, 390010-2 recall: The device does not bear a unique device identifier
The device does not bear a unique device identifier.
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Class II · 7 months ago
Altruan GmbH Brand Name: Bisaf Strep A Self-Test. Test for detection of group recall: Product not cleared by the FDA
Product not cleared by the FDA.
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Class II · 7 months ago
Medartis AG Brand Name: APTUS Product Name: 2.8 TriLock Screw 16mm, HD7 recall: Mix up between specified lots of 2.5mm and 2.8mm outer diameter screws
Mix up between specified lots of 2.5mm and 2.8mm outer diameter screws.
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Class II · 7 months ago
Waldemar Link GmbH & Co. KG Endo-Model SL Connection Component incl. PE-Plateau recall: The potential for an implant with a plateau screw where the bushing
The potential for an implant with a plateau screw where the bushing could detach from the screw shaft due to a longitudinal fracture.
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Class II · 7 months ago
Instrumentation Laboratory GEM Premier 5000 recall: Confirmed customer complaints indicating that GEM PAKs (cartridges)
Confirmed customer complaints indicating that GEM PAKs (cartridges) for the GEM Premier 5000 may experience an increased incidence of Process Control…
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Class II · 7 months ago
Instrumentation Laboratory GEM Premier 5000 PAK recall: Confirmed customer complaints indicating that GEM PAKs (cartridges)
Confirmed customer complaints indicating that GEM PAKs (cartridges) for the GEM Premier 5000 may experience an increased incidence of Process Control…
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Class II · 7 months ago
Instrumentation Laboratory GEM Premier 5000 PAK recall: Confirmed customer complaints indicating that GEM PAKs (cartridges)
Confirmed customer complaints indicating that GEM PAKs (cartridges) for the GEM Premier 5000 may experience an increased incidence of Process Control…
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Class II · 7 months ago
Lutronic Corporation Clarity II Laser System recall: Reports of devices sparking/popping and potentially burning patients
Reports of devices sparking/popping and potentially burning patients.
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Class II · 7 months ago
Medline Surgical Drapes: Mdtbtcs6070GN Dbd-Drape,Cover,Table recall: Fabric may experience premature delamination when using included laundering
Fabric may experience premature delamination when using included laundering instructions. Identifying delaminated gown or drape in a surgical setting…
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Class II · 7 months ago
Waldemar Link GmbH & Co. KG Endo-Model Replacement Plateau recall: The potential for an implant with a plateau screw where the bushing
The potential for an implant with a plateau screw where the bushing could detach from the screw shaft due to a longitudinal fracture.
-
Class II · 7 months ago
Waldemar Link GmbH & Co. KG Endo-Model SL Connection Component incl. PE-Plateau recall: The potential for an implant with a plateau screw where the bushing
The potential for an implant with a plateau screw where the bushing could detach from the screw shaft due to a longitudinal fracture.
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Class II · 7 months ago
Medline Medcrest Surgical Gowns: Mdtgxc4J5XL Dbq-Gown,Surg,Xalt recall: Fabric may experience premature delamination when using included laundering
Fabric may experience premature delamination when using included laundering instructions. Identifying delaminated gown or drape in a surgical setting…
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Class II · 7 months ago
Instrumentation Laboratory GEM Premier 5000 recall: Confirmed customer complaints indicating that GEM PAKs (cartridges)
Confirmed customer complaints indicating that GEM PAKs (cartridges) for the GEM Premier 5000 may experience an increased incidence of Process Control…
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Class II · 7 months ago
Waldemar Link GmbH & Co. KG Endo-Model Replacement Plateau recall: The potential for an implant with a plateau screw where the bushing
The potential for an implant with a plateau screw where the bushing could detach from the screw shaft due to a longitudinal fracture.
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Class II · 7 months ago
Ion Beam Applications S.A. IBA Proton Therapy System - Proteus 235 recall: It was identified that eh Universal Beam Triggering Interface (UBTI)
It was identified that eh Universal Beam Triggering Interface (UBTI) is disabled in the Therapy Safety System (TSS) configuration. In this condition…
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Class III · 7 months ago
Penner Pacific Bathing Spa, Model Numbers 350010-1, 350000-2, 350010-X recall: The device does not bear a unique device identifier
The device does not bear a unique device identifier.
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Class II · 7 months ago
Exactech, Inc. Brand Name: Equinoxe Product Name: Equinoxe Core Instrument Kit Model/ recall: Impactor handle may be missing cross-pin
Impactor handle may be missing cross-pin
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Class I · 7 months ago
Trividia Health, Inc. Owner's Booklets and Instructions for Use that are used recall: The system labeling (user manual and online labeling) did not provide
The system labeling (user manual and online labeling) did not provide adequate directions for lay users to act on the E-5 error code. The error code…