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
Becton Dickinson & Company 10mL Non-Sterile BD Luer-Lok Tip Syringe Only recall: During the bulk packaging process, some Luer Slip syringes were incorrectly
During the bulk packaging process, some Luer Slip syringes were incorrectly included in a batch designated for Luer Lok syringes.
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Class II · 7 months ago
Altruan GmbH Clearest Strep-A Cassette Test. Test to determine the presence of group recall: Product not cleared by the FDA
Product not cleared by the FDA.
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Class III · 7 months ago
Penner Pacific Bathing Spa, Model Numbers 560010-2L 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
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 III · 7 months ago
Penner Pacific Bathing Spa, Model Numbers 860010-1L 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
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 361910-1A recall: The device does not bear a unique device identifier
The device does not bear a unique device identifier.
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Class III · 7 months ago
Penner Pacific Bathing Spa, Model Numbers 360010-2WT 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
Covidien LLC HealthCast "Vital Sync" Remote Patient Monitoring System which consists recall: Due to complaints and investigations stating that alarms from the primary
Due to complaints and investigations stating that alarms from the primary patient bedside monitor was not alarming/being transmitted and received on…
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Class III · 7 months ago
Penner Pacific Bathing Spa, Model Numbers 760010-1, 770010-1 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
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
International Life Sciences Artelon FlexBand Plus Ref: 41054 & 41057 recall: Augmentation devices failed bacterial endotoxin testing
Augmentation devices failed bacterial endotoxin testing.
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Class II · 7 months ago
KOB GmbH Medline Unna-Z Stretch Zinc Paste Bandage recall: Due to labeling error. Incomplete ingredients listed. Labeling did
Due to labeling error. Incomplete ingredients listed. Labeling did not include castor oil or calamine.
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Class II · 7 months ago
International Life Sciences Artelon Flexband Twist .12 Ref: TW012 3.85x17mm HEX recall: Augmentation devices failed bacterial endotoxin testing
Augmentation devices failed bacterial endotoxin testing.
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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 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 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…
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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
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
Medartis AG Brand Name: APTUS Product Name: 2.5 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
Physio-Control, Inc. Physio Control Infant/Child Reduced Energy Defibrillator recall: Due to pediatric defibrillator electrode delamination
Due to pediatric defibrillator electrode delamination
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Class II · 7 months ago
Beckman Coulter Mishima K.K. DxC 700 AU, REF: B86444, B86446 recall: A delay in results may occur. When clinical chemistry analyzer calibration
A delay in results may occur. When clinical chemistry analyzer calibration monitor with PC installed with Microsoft SQL Server 2022 Express is open…