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. 2,710 recalls have been distributed to Florida in the last 12 months.
Showing 27061–27080 of 55,837 recalls
Recalled Item: ARTIS Pheno Interventional Fluoroscopic X-Ray System Recalled by Siemens...
The Issue: Temperature of the detector may fall out of its designed working range (cool...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Artis Q Interventional Fluoroscopic X-Ray System Recalled by Siemens Medical...
The Issue: Temperature of the detector may fall out of its designed working range (cool...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Stryker Sustainability Solutions (SSS) reprocessed Arthroscopic Shavers...
The Issue: Affected lots of reprocessed arthroscopic shavers may display the incorrect...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Sysmex XN-Series Fluorocell PLT Recalled by Sysmex America, Inc. Due to The...
The Issue: The fluorescent platelet counts (PLT-F) and immature platelet fraction (IPF)...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Valsartan 320 mg tablets Recalled by Bryant Ranch Prepack Inc. Due to CGMP...
The Issue: CGMP Deviations: Carcinogen impurity detected in API used to manufacture...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Valsartan 320 mg tablets Recalled by Bryant Ranch Prepack Inc. Due to CGMP...
The Issue: CGMP Deviations: Carcinogen impurity detected in API used to manufacture...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Valsartan 80 mg tablets Recalled by Bryant Ranch Prepack Inc. Due to CGMP...
The Issue: CGMP Deviations: Carcinogen impurity detected in API used to manufacture...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: TeaSource Roasted Chestnut Recalled by Teasource Due to Undeclared Slivered
The Issue: Roasted Chestnut loose leaf tea contains undeclared slivered almonds.
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: FP0692 Recalled by Confidence Inc./Confidence U.S.A. Inc. Due to Undeclared...
The Issue: Product contains undeclared ingredients, Hydroxypropyl Methylcellulose...
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: FP0391 Confidence Recalled by Confidence Inc./Confidence U.S.A. Inc. Due to...
The Issue: Product contains undeclared ingredients, Hydroxypropyl Methylcellulose...
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: FP0292 Confidence Nitro-Cross 60s Recalled by Confidence Inc./Confidence...
The Issue: Product contains undeclared ingredients, Hydroxypropyl Methylcellulose...
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Food Network Kitchen Inspirations Asian Style Sesame Ginger Dressing. 12...
The Issue: Consumer complaints of product spoilage. Per the manufacturer this issue is...
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: FP0392 Recalled by Confidence Inc./Confidence U.S.A. Inc. Due to Undeclared...
The Issue: Product contains undeclared ingredients, Hydroxypropyl Methylcellulose...
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Testosterone 200 mg Pellet Recalled by Right Value Drug Stores, Inc. Due to...
The Issue: Labeling: Incorrect or Missing Lot and/or Exp Date: Incorrect expiration...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: AMSCO V-PRO 1 Recalled by Steris Corporation Due to There is the potential...
The Issue: There is the potential for a scenario where a punctured cup of sterilant...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Li-ion battery packs used in BIS Vista and BIS View Recalled by Covidien LLC...
The Issue: Revised replacement instructions for the Li-ion battery packs used in BIS...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Hoffmann LRF Hexapod Software Catalog #: 983031 Software Version #: Recalled...
The Issue: When creating a correction plan with the Correct Axial First button selected...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: HYTEC Stop Solution (Allergy) Recalled by Hycor Biomedical LLC Due to Some...
The Issue: Some of the Stop Solution bottles, a caustic solution, have been reported to...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: PR1000 Pivot Rehab Bed AC powered adjustable bed. Recalled by Med-Mizer,...
The Issue: Under certain conditions, when pivoting bed to the extreme left there are...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Binding Site Human IgM Kit (for SPAPLUS) Recalled by The Binding Site Group,...
The Issue: After running the calibration curve, the recovery of the IgM kit control...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.