Recalls affecting Florida
Notices that name Florida in their distribution area, plus every nationwide recall — nationwide recalls reach Florida too.
-
Class III · 11 days ago
Mindray DS USA, Inc. BeneVision Series Telemetry Monitor. Operator's Manuals recall: Certain monitor operator's manuals contain descriptions
Certain monitor operator's manuals contain descriptions that may be insufficient or may require clarification regarding selected physiological alarm…
-
Class II · 11 days ago
AVID Medical, Inc. Davinci LAP/GYN recall: Product may be potentially contaminated with a lubricant used during
Product may be potentially contaminated with a lubricant used during the manufacturing process.
-
Class II · 11 days ago
Polymedco, Inc. / Polymedco Cancer Diagnostic Products, LLC Sediplast recall: During use of an affected tube, the operator may encounter increased
During use of an affected tube, the operator may encounter increased resistance when inserting the pipette. The resulting pressure buildup may cause…
-
Class II · 11 days ago
Beckman Coulter Inc. DxC 500i Clinical Analyzer Modules: 1. DxC 500 AU Module w/ISE recall: Beckman Coulter has identified a software issue affecting DxC 500i Clinical
Beckman Coulter has identified a software issue affecting DxC 500i Clinical Analyzers when testing plasma samples. Following user configuration of a…
-
Class III · 11 days ago
Mindray DS USA, Inc. Panorama and Telemetry Monitoring System. Operator's Manuals recall: Certain monitor operator's manuals contain descriptions
Certain monitor operator's manuals contain descriptions that may be insufficient or may require clarification regarding selected physiological alarm…
-
Class II · 11 days ago
AVID Medical, Inc. Major Pack recall: Product may be potentially contaminated with a lubricant used during
Product may be potentially contaminated with a lubricant used during the manufacturing process.
-
Class II · 11 days ago
AVID Medical, Inc. GYN Laparoscopy/Laparotomy recall: Product may be potentially contaminated with a lubricant used during
Product may be potentially contaminated with a lubricant used during the manufacturing process.
-
Class III · 11 days ago
Mindray DS USA, Inc. BeneVision N1 and N-Series Patient Monitor. Patient Monitor recall: Certain monitor operator's manuals contain descriptions
Certain monitor operator's manuals contain descriptions that may be insufficient or may require clarification regarding selected physiological alarm…
-
Class II · 11 days ago
AVID Medical, Inc. ABD Hysterectomy recall: Product may be potentially contaminated with a lubricant used during
Product may be potentially contaminated with a lubricant used during the manufacturing process.
-
Class II · 11 days ago
AVID Medical, Inc. GYN Laparoscopy Pack recall: Product may be potentially contaminated with a lubricant used during
Product may be potentially contaminated with a lubricant used during the manufacturing process.
-
Class II · 11 days ago
Medline Industries, LP Rollator, Bariatric, Basic Steel, Burgundy recall: The front fork stem bolt/wheel assembly may disconnect from the rollator
The front fork stem bolt/wheel assembly may disconnect from the rollator frame tubing. If the front fork stem bolt/wheel assembly disconnects from…
-
Class II · 11 days ago
Steris Corporation Verify Biological Steam Test Pack Model/ recall: Geobacillus stearothermophilus spore population in affected products may fall
Geobacillus stearothermophilus spore population in affected products may fall below minimum shelf life specification. When used to monitor steam…
-
Class II · 11 days ago
AVID Medical, Inc. Davinci Trucustom Bundle recall: Product may be potentially contaminated with a lubricant used during
Product may be potentially contaminated with a lubricant used during the manufacturing process.
-
Class III · 11 days ago
Mindray DS USA, Inc. ePM Series Patient Monitor. Patient Monitor Series: ePM 10M/ePM recall: Certain monitor operator's manuals contain descriptions
Certain monitor operator's manuals contain descriptions that may be insufficient or may require clarification regarding selected physiological alarm…
-
Class II · 11 days ago
AVID Medical, Inc. Urology Major recall: Product may be potentially contaminated with a lubricant used during
Product may be potentially contaminated with a lubricant used during the manufacturing process.
-
Class II · 11 days ago
Steris Corporation HexaVue Focus Integration System, a single recall: A software issue may result in unintended mismatch of patient information
A software issue may result in unintended mismatch of patient information on manually printed images. Incorrect patient information appearing on…
-
Class II · 11 days ago
AVID Medical, Inc. Craniotomy Pack recall: Product may be potentially contaminated with a lubricant used during
Product may be potentially contaminated with a lubricant used during the manufacturing process.
-
Class II · 11 days ago
Onkos Surgical Inc. My3D recall: Personalized pelvic implants inadvertently mixed up and distributed
Personalized pelvic implants inadvertently mixed up and distributed to incorrect customers.
-
Class II · 11 days ago
AVID Medical, Inc. Adult Heart Tray Shands Jacks recall: Product may be potentially contaminated with a lubricant used during
Product may be potentially contaminated with a lubricant used during the manufacturing process.
-
Class II · 11 days ago
Steris Corporation Verify Biological/Integrator Challenge Pack Model/ recall: Geobacillus stearothermophilus spore population in affected products may fall
Geobacillus stearothermophilus spore population in affected products may fall below minimum shelf life specification. When used to monitor steam…
-
Class II · 11 days ago
AVID Medical, Inc. Robotic Prostatectomy Pack recall: Product may be potentially contaminated with a lubricant used during
Product may be potentially contaminated with a lubricant used during the manufacturing process.
-
Class II · 11 days ago
Steris Corporation Verify Dual Species Self-Contained Biological Indicator Model/ recall: Geobacillus stearothermophilus spore population in affected products may fall
Geobacillus stearothermophilus spore population in affected products may fall below minimum shelf life specification. When used to monitor steam…
-
Class II · 11 days ago
Limitless Cryo Spa LLC Glypto Device, Glypto Cryo Machine recall: Lack of 510(k) clearance
Lack of 510(k) clearance.
-
Class II · 11 days ago
Steris Corporation Verify Dual Species Self-Contained Biological Indicator Model/ recall: Geobacillus stearothermophilus spore population in affected products may fall
Geobacillus stearothermophilus spore population in affected products may fall below minimum shelf life specification. When used to monitor steam…