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. 2,670 recalls have been distributed to Florida in the last 12 months.
Showing 38461–38480 of 55,837 recalls
Recalled Item: The Vesa 75/100 adaptation with rotation is an accessory to Recalled by...
The Issue: Supplier of the "VESA 75 / 100 adaptation with rotation", which is part of...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: New York Style Chocolate Iced ¿clairs under the following labels: Recalled...
The Issue: Products were recalled due to the potential presence of plastic foreign...
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Tina-Quant (Latex) HS Test System (C-Reactive Protein (Latex) High...
The Issue: Tina-quant Cardiac C-reactive Protein (Latex) High Sensitive (CRPHS) lot...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Fresenius Hemoflow F3 Dialyzer Part Number: 0520165A Indicated for Acute...
The Issue: Dialyzer header leak due to possible improper torque
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: The Symbia gamma camera system Product Usage: The Symbia gamma Recalled by...
The Issue: We received a customer complaint that Siemens reported via the MedWatch...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: The E.CAM gamma camera system Product Usage: The E.CAM gamma Recalled by...
The Issue: We received a customer complaint that Siemens reported via the MedWatch...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: system Recalled by Siemens Medical Solutions USA, Inc Due to In Artis zeego...
The Issue: In Artis zeego systems, angulations in the vicinity of the C-arm collision...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Spacelabs Healthcare Xhibit Central Station Recalled by Spacelabs Healthcare...
The Issue: The firm has received one report of values for patient height and weight...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Telmisartan Tablets Recalled by Torrent Pharmaceuticals Limited Due to...
The Issue: Presence of Foreign Substance: Product complaint for the presence of foreign...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: TeleSentry Battery Recalled by Scottcare Corporation Due to The firm...
The Issue: The firm received a complaint of the battery exploding while recharging.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: 30" (76 cm) Appx. 3.3 ml Recalled by ICU Medical, Inc. Due to ICU Medical...
The Issue: ICU Medical has identified an issue with a connection in an isolated number...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: 30" (76 cm) Appx. 6.3 ml Recalled by ICU Medical, Inc. Due to ICU Medical...
The Issue: ICU Medical has identified an issue with a connection in an isolated number...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: 30" (76 cm) Appx. 3.3 ml Recalled by ICU Medical, Inc. Due to ICU Medical...
The Issue: ICU Medical has identified an issue with a connection in an isolated number...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: 31" (79 cm) Appx. 3.4 ml Recalled by ICU Medical, Inc. Due to ICU Medical...
The Issue: ICU Medical has identified an issue with a connection in an isolated number...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: 30" (76 cm) Appx 3.6 ml Recalled by ICU Medical, Inc. Due to ICU Medical has...
The Issue: ICU Medical has identified an issue with a connection in an isolated number...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: 110" (279 cm) Appx 13.8 ml Recalled by ICU Medical, Inc. Due to ICU Medical...
The Issue: ICU Medical has identified an issue with a connection in an isolated number...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: 74" (188cm) approximately 9.0ml Recalled by ICU Medical, Inc. Due to ICU...
The Issue: ICU Medical has identified an issue with a connection in an isolated number...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: 30" (76 cm) Appx 6.3 ml Recalled by ICU Medical, Inc. Due to ICU Medical has...
The Issue: ICU Medical has identified an issue with a connection in an isolated number...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: PureWick External Catheter for Women-Wick Product Usage: A flexible Recalled...
The Issue: PureWick is recalling external catheter for women Wicks because the labeling...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Toshiba America Medical Systems Angio WorkStation: XIDF-AWS801v6.00 Recalled...
The Issue: During a procedure the Peak Skin Dose (PSD) value was displayed on the DTS...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.