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 12501–12520 of 30,087 recalls
Recalled Item: Gentell Hydrogel Ag 4oz. Tube Recalled by Gentell, Inc Due to During an FDA...
The Issue: During an FDA audit, it was discovered that the product was not properly...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: NAVIO Soft Tissue Protector Recalled by Smith & Nephew, Inc. Due to...
The Issue: Potential for the NAVIO Soft Tissue Protector to become stuck or bound to...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Gentell Hydrogel Ag 2x2 Recalled by Gentell, Inc Due to During an FDA audit,...
The Issue: During an FDA audit, it was discovered that the product was not properly...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Gentell Hydrogel Ag 4x8 Recalled by Gentell, Inc Due to During an FDA audit,...
The Issue: During an FDA audit, it was discovered that the product was not properly...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: The CapsoCam Plus (SV-3) Recalled by Capso Vision, Inc. Due to Ingestible...
The Issue: Ingestible video capsule system has capsule with incorrect capture mode...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: BARD MYPICC KIT 3F Single-Lumen Recalled by Becton Dickinson & Company Due...
The Issue: The kits contain surgical gowns which were subject to a recall by the supplier.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: BARD MYPICC KIT 5F Dual-Lumen Recalled by Becton Dickinson & Company Due to...
The Issue: The kits contain surgical gowns which were subject to a recall by the supplier.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: BARD MYPICC KIT 5F Dual-Lumen Recalled by Becton Dickinson & Company Due to...
The Issue: The kits contain surgical gowns which were subject to a recall by the supplier.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: BARD MYPICC KIT 5F Triple-Lumen Recalled by Becton Dickinson & Company Due...
The Issue: The kits contain surgical gowns which were subject to a recall by the supplier.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: BARD MYPICC KIT 4F Single-Lumen Recalled by Becton Dickinson & Company Due...
The Issue: The kits contain surgical gowns which were subject to a recall by the supplier.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: BARD MYPICC KIT 5F Triple-Lumen Recalled by Becton Dickinson & Company Due...
The Issue: The kits contain surgical gowns which were subject to a recall by the supplier.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: BARD MYPICC KIT 4F Dual-Lumen Recalled by Becton Dickinson & Company Due to...
The Issue: The kits contain surgical gowns which were subject to a recall by the supplier.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: BARD MYPICC KIT 5F Dual-Lumen Recalled by Becton Dickinson & Company Due to...
The Issue: The kits contain surgical gowns which were subject to a recall by the supplier.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: HeartStart MRx Monitor/Defibrillators with model numbers M3535A M3536A...
The Issue: Philips has received a number of reports of HeartStart MRx...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Nexus Universal with OptiBond Universal Recalled by Kerr/Pentron, DBA Kerr...
The Issue: An issue within production process used to package trial kits let to the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Butterfly iQ Ultrasound System Auto Bladder Volume Tool-The Auto Bladder...
The Issue: Distributed without an approved 510(k)
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Butterfly iQ Ultrasound System containing the Auto EF(Ejection Fraction)...
The Issue: Distributed without an approved 510(k)
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: LivaNova Heater-Cooler System 3T - Product Usage: The Heater-Cooler 3T...
The Issue: The firm is providing validated cleaning and disinfection instructions in...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: R-F Injector Cannula. 18gx10cm-STERILE. REF/UDI: 257-1810/(01)00828788021496...
The Issue: Incorrect expiration date on introduction cannula packaging.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: R-F Injector Cannula. 20gx10cm-STERILE. REF/UDI: 257-2010/(01)10818788022124...
The Issue: Incorrect expiration date on introduction cannula packaging.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.