Recalls affecting Florida
Notices that name Florida in their distribution area, plus every nationwide recall — nationwide recalls reach Florida too.
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Class II · 8 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 · 8 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 · 8 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 · 8 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 · 8 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 II · 8 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 · 8 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 · 8 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 · 8 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 · 8 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 · 8 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 · 8 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 · 8 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 · 8 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 · 8 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 · 8 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 · 8 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 · 8 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 · 8 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…
-
Class II · 8 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…
-
Class II · 8 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…
-
Class II · 8 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…
-
Class II · 8 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…
-
Class II · 8 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…