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. 2,769 recalls have been distributed to Ohio in the last 12 months.
Showing 6721–6740 of 30,087 recalls
Recalled Item: RR Mechatronics Control Level A ESR Control4.6 ml QRR049002- In-vitro...
The Issue: QRR049001 Lot QCAB6AN505 incorrectly labelled as QRR049002 Lot QCAB6AAA28....
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: VITROS Chemistry Products Calibrator Kit 11 VANC Reagent Generation (GEN)...
The Issue: Unavailable to calibrate VITROS Chemistry Products VANC Reagent, Generation...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: DePuy Mitek BIOKNOTLESS Plus w/ Panacryl-Indicated for use in soft Recalled...
The Issue: IFU Warning: Applying bending force and/or bending force with impaction to...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: DePuy Mitek BIOKNOTLESS Plus w/ OC-Indicated for use in soft Recalled by...
The Issue: IFU Warning: Applying bending force and/or bending force with impaction to...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: DePuy Mitek BIOKNOTLESS Rapid W/ OC-Indicated for use in soft Recalled by...
The Issue: IFU Warning: Applying bending force and/or bending force with impaction to...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: DePuy Mitek BIOKNOTLESS Plus w/ Ethibond-Iindicated for use in soft Recalled...
The Issue: IFU Warning: Applying bending force and/or bending force with impaction to...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: DePuy Mitek BIOKNOTLESS Rapid w/ Pan-Indicated for use in soft Recalled by...
The Issue: IFU Warning: Applying bending force and/or bending force with impaction to...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: TRIATHLON X3 TIBIAL BEARING INSERT PS #4 13MM Intended for Recalled by...
The Issue: Mislabeled:Labeled Catalog Number: 5531-G-312-E, TRIATHLON X3 TIBIAL BEARING...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: TRIATHLON X3 TIBIAL BEARING INSERT CS #3 12MM-Intended for knee Recalled by...
The Issue: Mislabeled:Labeled Catalog Number: 5531-G-312-E, TRIATHLON X3 TIBIAL BEARING...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Teleflex (manufacturer: Vascular SOLUTIONS) D-Stat Flowable Hemostat...
The Issue: The product contains an expired diluent vial. If the impacted product is...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Ultraview SL (UVSL) Command Module Recalled by Spacelabs Healthcare, Inc....
The Issue: Command modules will display the following when parameter processing is...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: StealthStation Cranial Software Recalled by Medtronic Navigation, Inc. Due...
The Issue: During non-axial/some axial exams, software anomalies occur during...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Bard Mission Disposable Core Biopsy Instrument Kit: Recalled by Bard...
The Issue: Coaxial cannula internal diameter and length of biopsy instruments exceed...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Henry Schein Hard Line Chairside Reline kit-Resilient Acrylic Denture...
The Issue: The Hard Line Chairside Reline Kit (570-0718) (0921940HS) was labeled as...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Over-Head Ceiling Tube Support Recalled by SHIMADZU CORPORATION MEDICAL...
The Issue: Eight fixing bolts at the base of the X-ray ceiling tube column assembly may...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Reliance Vision Multi-Chamber Washer/Disinfector Recalled by Steris...
The Issue: In the remote occurrence in which the electrical contactor component present...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: stryker ORTHOLOC 3Di Fusion Plate MTP Right Recalled by Wright Medical...
The Issue: Two lots of Ortholoc 3Di Fusion plates contain incorrect dorsiflexion...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: stryker ORTHOLOC 3Di Fusion Plate MTP Right Recalled by Wright Medical...
The Issue: Two lots of Ortholoc 3Di Fusion plates contain incorrect dorsiflexion...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Cytrellis ellacor System with Micro-Coring Technology-Dermal Micro-Coring...
The Issue: Irregular core patterns could cause potential overlap of cores at the 8%...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Blue Rhino G2-Multi Percutaneous Tracheostomy Introducer Tray Recalled by...
The Issue: There were reports from customers that the tracheostomy in the sets and...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.