Product Recalls in Florida
Product recalls affecting Florida — including food, drugs, consumer products, medical devices, and vehicles distributed to Florida. RecallDetector monitors distribution data from the FDA, USDA, CPSC, and NHTSA to show you which recalls are relevant to your area. 2,739 recalls have been distributed to Florida in the last 12 months.
Showing 21421–21440 of 30,686 recalls
Recalled Item: Image1 SPIES X-LINK Camera Control Unit (CCU) Recalled by Karl Storz...
The Issue: Potential electrical interference issue when the Image1 SPIES X-LINK and...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: PoleStar system (N20 / N30) Warning Lamps Control Box Recalled by Medtronic...
The Issue: Medtronic Navigation is recalling certain components of the PoleStar system...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ADVIA¿ Chemistry (Syva Onboard) Theophylline_2 (THEO_2) Reagent is for in...
The Issue: Siemens Healthcare Diagnostics has confirmed the Syva¿ EMIT¿ 2000...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Achillon Minimally Invasive Device for Achilles Tendon Rupture Treatment The...
The Issue: Data from internal studies suggests there may be a potential that the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: MOSAIQ Oncology Information System Recalled by Elekta, Inc. Due to It is...
The Issue: It is possible that that the selected Plan-of-the Day could be accidently...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Syva¿ EMIT¿ 2000 Theophylline - Catalog # 4P019UL /SMN#10445324 is Recalled...
The Issue: Siemens Healthcare Diagnostics has confirmed the Syva¿ EMIT¿ 2000...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: AB SCIEX Triple Quad 4500MD LC/MS/MS System. Mass Spectrometer for Recalled...
The Issue: MultiQuant MD software where under certain conditions a user can be...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: AB Sciex API 3200MD" LC/MS/MS System. In-Vitro Diagnostic Instrument Part...
The Issue: MultiQuant MD software where under certain conditions a user can be...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Medtronic Recalled by Medtronic Inc., Cardiac Rhythm and Heart Failure Due...
The Issue: This Pacing Lead System does not comply with Section 8.5.2.3 of IEC 60601-1,...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: AB SCIEX QTRAP¿ 4500MD LC/MS/MS System Mass Spectrometer for In-Vitro...
The Issue: MultiQuant MD software where under certain conditions a user can be...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: AB SCIEX 3200MD QTRAP¿ LC/MS/MS System Mass Spectrometer for In-Vitro...
The Issue: MultiQuant MD software where under certain conditions a user can be...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: A7 Anesthesia Delivery System Recalled by Mindray DS USA, Inc. dba Mindray...
The Issue: Potential for a leak to occur on the back-up O2 and air e-size cylinder...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Smith and Nephew TWINFIX QUICK-T Knot Pusher Suture Cutter Recalled by Smith...
The Issue: The device could be subject to breaches of its sterile packaging.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Anspach G1 High Speed Electric Handpiece Air Cooled (eG1A) Use Recalled by...
The Issue: The graphics at the attachment interface indicating locked and unlocked...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: T030-000 -30" 20 Drop IV Admin Secondary Set. Packaged in a Tyvek pouch...
The Issue: WalkMed Infusion, LLC Announces a Voluntary Field Action of Multiple Triton...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: T100-022F with 0.22 micron filter and FP Clip. Packaged in a Tyvek pouch...
The Issue: WalkMed Infusion, LLC Announces a Voluntary Field Action of Multiple Triton...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: T095-120 IV Set with 1.2 Micron Filter. Packaged in a Tyvek pouch Recalled...
The Issue: WalkMed Infusion, LLC Announces a Voluntary Field Action of Multiple Triton...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Spike Set Recalled by WalkMed Infusion, LLC Due to WalkMed Infusion, LLC...
The Issue: WalkMed Infusion, LLC Announces a Voluntary Field Action of Multiple Triton...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: The pump (with cushioning foam inserts) is packaged in a Recalled by WalkMed...
The Issue: WalkMed Infusion, LLC Announces a Voluntary Field Action of the Triton...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Stryker AutoPlex System. Model Numbers 0607-687-000 Recalled by Stryker...
The Issue: The Piston Head can become separated from the Delivery Piston, blocking the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.