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. 1,075 recalls have been distributed to Florida in the last 12 months.
Showing 17701–17720 of 55,837 recalls
Recalled Item: HALOPERIDOL TABLETS 20mg Recalled by Cardinal Health Inc. Due to CGMP...
The Issue: CGMP Deviations: Intermittent exposure to temperature excursion during storage.
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: ZOMA-Jet 10 Demonstration Kit Recalled by Ferring Pharmaceuticals Inc Due to...
The Issue: Defective Delivery System: customer complaints concerning the injector pen...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Omeprazole Delayed-Release Capsules Recalled by Breckenridge Pharmaceutical,...
The Issue: Failed Impurities/Degradation Specifications: Out-of-Specification results...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Phenylephrine HCl Injection Recalled by Sagent Pharmaceuticals Inc Due to...
The Issue: Lack of Assurance of Sterility: customer complaints of loose crimped vial...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: ZOMA-Jet 5 Demonstration Kit Recalled by Ferring Pharmaceuticals Inc Due to...
The Issue: Defective Delivery System: customer complaints concerning the injector pen...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Dasky Disposable Sampling Tube Recalled by Krishe Inc Due to Verification...
The Issue: Verification and validation of the virus transport medium tubes was not...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Tibial Opening Wedge Osteotomy Plate Recalled by Arthrex, Inc. Due to It was...
The Issue: It was discovered that five AR-13200ST-15.0 parts were processed as...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Tritanium X TL Instruments - intervertebral fusion device with bone graft...
The Issue: Stryker identified non-conforming instruments that are components of the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: HydraVision Digital Imaging System Product ID/Reorder Number: 705559 (65KW)...
The Issue: Failure to comply with the performance standard for fluoroscopy systems. Per...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Dasky Disposable Sampling Tube Recalled by Krishe Inc Due to Verification...
The Issue: Verification and validation of the virus transport medium tubes was not...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Dasky Disposable Sampling Tube Recalled by Krishe Inc Due to Verification...
The Issue: Verification and validation of the virus transport medium tubes was not...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Disposable Sampling Tube Recalled by Krishe Inc Due to Verification and...
The Issue: Verification and validation of the virus transport medium tubes was not...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: AngioDynamics SafeSheath ULTRALITE 10F Recalled by Oscor, Inc. Due to...
The Issue: Potential for open seal on sterile product
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Remel Haemophilus Test Medium (150 mm) 10/PK Recalled by Remel Inc Due to...
The Issue: When tested with H. influenza ATCC 49247 and ATCC 49766 both organisms may...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Remel Haemophilus Test Medium(100mm) 10/PK Recalled by Remel Inc Due to When...
The Issue: When tested with H. influenza ATCC 49247 and ATCC 49766 both organisms may...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Ysio X.pree Recalled by Siemens Medical Solutions USA, Inc Due to A patient...
The Issue: A patient image was assigned to a different patient during image recovery...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: CHINA_GEL (Camphor 3.00% Recalled by China Gel Inc Due to CGMP deviations:...
The Issue: CGMP deviations: Product being recalled as it was made in the same facility...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Durisan Antimicrobial Solutions (benzalkonium chloride) Hand Sanitizer...
The Issue: Microbial Contamination of Non-Sterile Products: firm's internal testing...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: heal the world Recalled by PNHC, LLC. Due to Labeling Not Elsewhere...
The Issue: Labeling Not Elsewhere Classified: Hand sanitizer packaged in containers...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: CHINA-GEL WHITE (Camphor 3.00% Recalled by China Gel Inc Due to CGMP...
The Issue: CGMP deviations: Product being recalled as it was made in the same facility...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.