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. 1,942 recalls have been distributed to Florida in the last 12 months.
Showing 28461–28480 of 55,837 recalls
Recalled Item: MegaPower Electrosurgical Generator Recalled by Megadyne Medical Products,...
The Issue: If two devices are plugged into the same channel/port in the generator, both...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: XLTEK EMU40EX EEG Headbox Recalled by Natus Neurology DBA Excel Tech., Ltd....
The Issue: Possible degradation of an internal electronic component over time which may...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Draeger Jaundice Meter JM-103 The device is intended for use in hospitals...
The Issue: Users have misinterpreted the display for out of range measurement indicated...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Draeger Jaundice Meter JM-105 The device is intended for use in hospitals...
The Issue: Users have misinterpreted the display for out of range measurement indicated...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Minicon Clinical Sample Concentrators for In Vitro Diagnostic Use 9031...
The Issue: In vitro diagnostic devices, used greater than 6 months after date of...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: O-Two Equinox¿ Relieve N2O/O2 Analgesic Gas Mixing and Delivery System...
The Issue: Higher levels of nitrous oxide delivered than specification
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: AdvanDx QuickFISH Slides Recalled by Opgen Inc Due to Possible diminished...
The Issue: Possible diminished performance prior to its established expiration date.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Safety Sideport Knife 1.0mm 45¿ Recalled by Beaver Visitec Due to Blades are...
The Issue: Blades are loose in handles and may fall out due to non cured epoxy
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Scopolamine Transdermal Therapeutic System Recalled by L. Perrigo Company...
The Issue: Defective delivery system
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Multi-Lumen Central Venous Catheterization Set with Blue FlexTip Catheter...
The Issue: The recalling firm has received complaints related to increased resistance...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Olympus JF-140F duodenoscopes (Model NumberJF-140F) Recalled by Olympus...
The Issue: Issuance of validated, new reprocessing procedures. This corrective action...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Olympus JF-160F duodenoscopes (Model NumberJF-160F) Recalled by Olympus...
The Issue: Issuance of validated, new reprocessing procedures. The new cleaning...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Vanguard Knee System PS Tibial Bearing Recalled by Zimmer Biomet, Inc. Due...
The Issue: The label master file was errantly set up as a 63/37mm instead of a 63/67mm....
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Alfalfa Seeds Recalled by Caudill Sprouting LLC Due to Potential Salmonella...
The Issue: The firm's seeds have been linked in a multistate outbreak of Salmonella...
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Outer Package Label: Tapered Screw-Vent Implant System Recalled by Zimmer...
The Issue: Dental implants have incorrect item/lot numbers and size on the inner...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Rio System Irrigation Clip - Catalog # 111690 Product Usage: Recalled by...
The Issue: Out of tolerance.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: GIBCO CTS AIM V Serum-Free Media (SFM) Recalled by Life Technologies, Corp....
The Issue: It has been determined that the fill port tube seal integrity was...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Gibco Dulbecco's Modified Eagle Medium (DMEM) Recalled by Life Technologies,...
The Issue: It has been determined that the fill port tube seal integrity was...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Gibco CTS OpTmizer T Cell Expansion Serum Free Medium Recalled by Life...
The Issue: It has been determined that the fill port tube seal integrity was...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Gibco Dulbecco's Modified Eagle Medium (DMEM) Recalled by Life Technologies,...
The Issue: It has been determined that the fill port tube seal integrity was...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.