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. 2,487 recalls have been distributed to Ohio in the last 12 months.
Showing 45861–45880 of 55,415 recalls
Recalled Item: Ferrous Gluconate Tablets Recalled by National Vitamin Co Inc Due to Mislabeling
The Issue: National Vitamin is recalling Nature's Blend Ferrous Gluconate Tablets...
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: ROSA Surgical Device 2.5.8 It is intended to be used Recalled by Zimmer...
The Issue: Software corrections reactivating the cooperative endoscopy mode.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: DeRoyal Cardiac Hypothermia Tray Recalled by DeRoyal Industries Inc Due to...
The Issue: The firm distributed surgical kits which contained Irrigation Sets which...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: DeRoyal KNEE ARTHROSCOPY PACK Recalled by DeRoyal Industries Inc Due to The...
The Issue: The firm distributed surgical kits which contained Irrigation Sets which...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: InTouch Critical Care Bed Recalled by Stryker Medical Division of Stryker...
The Issue: Stryker has received complaints from the field alleging instances where the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: PALL Medical Breathing Circuit Filter Recalled by Pall Corporation Due to...
The Issue: Possible leak from the filter allowing a small of amount of air to be...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Stride Femoral Component Size 2 Recalled by Blue Belt Technologies MN Due to...
The Issue: Mislabeled. Packages labeled PFSI-00053, Right Lateral/Left Medial contains...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Stride Femoral Component Size 2 Recalled by Blue Belt Technologies MN Due to...
The Issue: Mislabeled. Packages labeled PFSI-00053, Right Lateral/Left Medial contains...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Model Number(s): PB840 Ventilator (4-840120DIUU-XX). The product is a...
The Issue: In the case of a loss of GUI display due to a Backlight Inverter PCBA...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: eye-pak 7407 Tray Support Cover Recalled by Alcon Research, Ltd. Due to The...
The Issue: The peel pouches of the Tray Support Covers may be insufficiently sealed so...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: RECLAIM DISTAL TAPERED Recalled by DePuy Orthopaedics, Inc. Due to The...
The Issue: The product can be difficult to remove from the Distal Stem both out of the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: RECLAIM Taper Protector Sleeve. RECLAIM Revision Hip System Orthopedic...
The Issue: The product can be difficult to remove from the Distal Stem both out of the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: RECLAIM DISTAL TAPERED Distal Stem Recalled by DePuy Orthopaedics, Inc. Due...
The Issue: The product can be difficult to remove from the Distal Stem both out of the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ACL TOP 500 CTS Recalled by Instrumentation Laboratory Co. Due to Potential...
The Issue: Potential for sample misidentification.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ACL TOP (Base) Recalled by Instrumentation Laboratory Co. Due to Potential...
The Issue: Potential for sample misidentification.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ACL TOP 700 Recalled by Instrumentation Laboratory Co. Due to Potential for...
The Issue: Potential for sample misidentification.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ACL TOP 700 LAS Recalled by Instrumentation Laboratory Co. Due to Potential...
The Issue: Potential for sample misidentification.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ACL TOP 700 CTS Recalled by Instrumentation Laboratory Co. Due to Potential...
The Issue: Potential for sample misidentification.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ACL TOP 300 CTS Recalled by Instrumentation Laboratory Co. Due to Potential...
The Issue: Potential for sample misidentification.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ACL TOP CTS Recalled by Instrumentation Laboratory Co. Due to Potential for...
The Issue: Potential for sample misidentification.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.