Product Recalls in Ohio
Product recalls affecting Ohio — including food, drugs, consumer products, medical devices, and vehicles distributed to Ohio. RecallDetector monitors distribution data from the FDA, USDA, CPSC, and NHTSA to show you which recalls are relevant to your area. 2,731 recalls have been distributed to Ohio in the last 12 months.
Showing 12561–12580 of 30,087 recalls
Recalled Item: Medline Winged Sponges Presaturated W/PVP DYND70289H Expiration 06/30/2022....
The Issue: Voids were discovered in the packaging seal and loss of sterility on the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: AGFA Digital Radiography X- Ray system DR 800 with TomoSynthesis- Recalled...
The Issue: Tomosynthesis image acquisition sequence did not stop automatically after...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Ysio Recalled by Siemens Medical Solutions USA, Inc Due to The Ysio system...
The Issue: The Ysio system may process incorrect internal values for the position of...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Getinge 88-Series-washer disinfectors intended for cleaning Recalled by...
The Issue: Potential leakage that may occur due to ruptured spot welds in the chamber,...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Kits containing Covidien Force TriVerse Electrosurgical Devices. Distributed...
The Issue: Sterile packaging may potentially be compromised, and use of products may...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Covidien Force TriVerse Electrosurgical Devices Recalled by Covidien Llc Due...
The Issue: Sterile packaging may potentially be compromised, and use of products may...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: NeuraGen Nerve Guide Recalled by Integra LifeSciences Corp. Due to...
The Issue: Nonconforming product which was dispositioned for rejection was mistakenly...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Elecsys CA 19-9 Recalled by Roche Diagnostics Operations, Inc. Due to The...
The Issue: The firm has received an increased number of complaints concerning...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Monitor for the Functional Imaging System for Magnetic Resonance Imaging...
The Issue: Insufficient shielding of Philips SensaVue DVI Adapter for computer monitor.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: IMMULITE 2000 Systems E2 Estradiol Catalog #: US: L2KE22(D) (200 Recalled by...
The Issue: Due to high discordant Estradiol results which.potentially affects all...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: IMMULITE 1000 Systems E2 Estradiol Catalog #: US: LKE21(D) and Recalled by...
The Issue: Due to high discordant Estradiol results which.potentially affects all...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: HEMO-7 Hemospray Endoscopic Hemostat Recalled by Wilson-Cook Medical Inc....
The Issue: Complaints that the handle and/or activation knob on Hemostat devices have...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: HEMO-10 Hemospray Endoscopic Hemostat Recalled by Wilson-Cook Medical Inc....
The Issue: Complaints that the handle and/or activation knob on Hemostat devices have...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: VNS Therapy Programmer Recalled by LivaNova USA Inc Due to False positive...
The Issue: False positive warning may occur after: 1) VNS Generator interrogated at 0mA...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: CareFusion Alaris System Recalled by CareFusion 303, Inc. Due to 1)Error...
The Issue: 1)Error 255-XX-XXX results in inability to edit settings 2)Delay options...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: CareFusion Alaris PCA Module Recalled by CareFusion 303, Inc. Due to 1)Error...
The Issue: 1)Error 255-XX-XXX results in inability to edit settings 2)Delay options...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: CareFusion Alaris Pump Module Recalled by CareFusion 303, Inc. Due to...
The Issue: 1)Error 255-XX-XXX results in inability to edit settings 2)Delay options...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: CareFusion Alaris Syringe Module Recalled by CareFusion 303, Inc. Due to...
The Issue: 1)Error 255-XX-XXX results in inability to edit settings 2)Delay options...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ABL90 FLEX PLUS Analyzer Recalled by Radiometer Medical ApS Due to The firm...
The Issue: The firm received reports of occurrences where the barcode reader...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ABL90 FLEX Analyzer Recalled by Radiometer Medical ApS Due to The firm...
The Issue: The firm received reports of occurrences where the barcode reader...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.