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. 2,939 recalls have been distributed to Florida in the last 12 months.
Showing 3041–3060 of 30,686 recalls
Recalled Item: SURG PAT XRAY 1X1 Model/Catalog Number: 801403. The surgical patties...
The Issue: Identified higher-than-expected levels of endotoxin within the raw material...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Chameleon PTA Balloon Catheter with Injection Port 5mm x 40mm Recalled by...
The Issue: Specific lots of the Chameleon PTA Balloon Catheter failed to meet in-house...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: AD-TECH Spencer Probe Depth Electrode Recalled by Ad-Tech Medical Instrument...
The Issue: Ad-Tech is recalling these A-Style SD Depth Electrodes because a label...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: AD-TECH Spencer Probe Depth Electrode Recalled by Ad-Tech Medical Instrument...
The Issue: Ad-Tech is recalling these A-Style SD Depth Electrodes because a label...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: AD-TECH Spencer Probe Depth Electrode Recalled by Ad-Tech Medical Instrument...
The Issue: Ad-Tech is recalling these A-Style SD Depth Electrodes because a label...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Brand Name: EVIS EXERA III Gastrointestinal Videoscope GIF-1TH190 Product...
The Issue: To better define the drying procedures described in the IFU to improve the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Medtronic Recharger Kits Recalled by Medtronic Neuromodulation Due to The...
The Issue: The Wireless Rechargers in the kits may be unable to enter a recharging...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Nihon Kohden Adult Ear Clip SpO2 Sensor Recalled by Nihon Kohden America Inc...
The Issue: Due to oximeters not having FDA market approval or clearance to distribute...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Nihon Kohden Adult/Pediatric Forehead Disposable SpO2 Sensor Recalled by...
The Issue: Due to oximeters not having FDA market approval or clearance to distribute...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: a. Hillrom Centrella Smart+ Medical-Surgical Hospital Bed Recalled by Baxter...
The Issue: The beds have a potential for an interface issue with the Rauland Responder...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: A1CNow+ Multi-Test HbA1c System consists of (1) a semi-disposable...
The Issue: The reason for this recall is PTS Diagnostics, Inc. received complaints of...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: The IMAGEnet 6 Ophthalmic Data System is a software program Recalled by...
The Issue: The overlay of visual field test locations on a probability map, as...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Saphena Medical Venapax XL- Endoscopic Vessel Harvesting System for use...
The Issue: A Gen 5 tail piece was assembled to a Gen 4 Finished Device, resulting in a...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Quantimetrix Urine Chemistry Control Set Dipper Urinalysis Dipstick Testing...
The Issue: The Quantimetrix Dipper Urinalysis Dipstick control was shipped without the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Phasitron5 Breathing Circuit (P5-10 Recalled by Percussionaire Corporation...
The Issue: As a result of product complaints, breathing circuits are experiencing...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Ambu¿ VivaSight 2 DLT Endobronchial tube Recalled by Ambu Inc. Due to Ambu...
The Issue: Ambu has received complaints on Ambu¿ VivaSight 2 DLTs regarding hyper...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ClariTEE Probe- Miniature transesophageal echo ultrasound probe for use with...
The Issue: Epoxy used to seal the edge of the transducer into its paddle exceeded...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Olympus Cystoscope Outer Sheath Recalled by Olympus Corporation of the...
The Issue: Product being removed due to incompatibility when used in conjunction with a...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Brand Name: Olympus Product Name: Cystoscope Outer Sheath Model/Catalog...
The Issue: Olympus is removing the statement of compatibility with a GreenLight Laser...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: EZDilate Wire Guided Balloon- Indicated for use in adult and Recalled by...
The Issue: Mislabeled Glo Cath Label (attached to the device) states: 11 mm, 12 mm, 13...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.