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. 2,790 recalls have been distributed to Ohio in the last 12 months.

55,415 total recalls
2,790 in last 12 months

Showing 36613680 of 30,087 recalls

Medical DeviceJuly 2, 2024· Zimmer, Inc.

Recalled Item: CPT Hip Joint Metal/Polymer Semi-Constrained Cemented Prosthesis Recalled by...

The Issue: Affected product has an increased risk of postoperative perisprosthetic...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceJuly 1, 2024· W L Gore & Associates, Inc.

Recalled Item: Heparin Recalled by W L Gore & Associates, Inc. Due to Due to packaging...

The Issue: Due to packaging defects, sterility assurance and heparin activity may be...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceJuly 1, 2024· W L Gore & Associates, Inc.

Recalled Item: Heparin Recalled by W L Gore & Associates, Inc. Due to Due to packaging...

The Issue: Due to packaging defects, sterility assurance and heparin activity may be...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceJuly 1, 2024· Neurovision Medical Products Inc

Recalled Item: Cobra Recalled by Neurovision Medical Products Inc Due to Mislabeling

The Issue: mislabeling; EMG RLN monitoring kit labeling contains the incorrect tube size.

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceJuly 1, 2024· Olympus Corporation of the Americas

Recalled Item: The Everest Bipolar Cutting Forceps are intended to be passed Recalled by...

The Issue: Fractures and breakages in packaging trays and Tyvek covers, which may...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceJuly 1, 2024· Olympus Corporation of the Americas

Recalled Item: The Everest Bipolar Cutting Forceps are intended to be passed Recalled by...

The Issue: Fractures and breakages in packaging trays and Tyvek covers, which may...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceJuly 1, 2024· Olympus Corporation of the Americas

Recalled Item: The Everest Bipolar Cutting Forceps are intended to be passed Recalled by...

The Issue: Fractures and breakages in packaging trays and Tyvek covers, which may...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceJune 28, 2024· Philips North America Llc

Recalled Item: IntelliVue Patient Monitor MX500 with L.x and M.x Recalled by Philips North...

The Issue: Philips lntelliVue Patient Monitors MX400/450/500/550 Shipped or Upgraded...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceJune 28, 2024· Philips North America Llc

Recalled Item: IntelliVue Patient Monitor MX400 with L.x and M.x Recalled by Philips North...

The Issue: Philips lntelliVue Patient Monitors MX400/450/500/550 Shipped or Upgraded...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceJune 28, 2024· Baxter Healthcare Corporation

Recalled Item: Baxter PST 500 U Recalled by Baxter Healthcare Corporation Due to Baxter...

The Issue: Baxter Healthcare Corporation is issuing an Urgent Medical Device Correction...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceJune 28, 2024· Philips North America Llc

Recalled Item: IntelliVue Patient Monitor MX450 with L.x and M.x Recalled by Philips North...

The Issue: Philips lntelliVue Patient Monitors MX400/450/500/550 Shipped or Upgraded...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceJune 28, 2024· Philips North America Llc

Recalled Item: IntelliVue Patient Monitor MX550 with L.x and M.x Recalled by Philips North...

The Issue: Philips lntelliVue Patient Monitors MX400/450/500/550 Shipped or Upgraded...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceJune 27, 2024· MEDLINE INDUSTRIES, LP - Northfield

Recalled Item: Medline convenience kits containing semi-rigid suction liners labeled as...

The Issue: XXX

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceJune 27, 2024· MEDLINE INDUSTRIES, LP - Northfield

Recalled Item: Medline convenience kits containing semi-rigid suction liners labeled as...

The Issue: Due to reported adverse events, Medline Industries, LP. is issuing a recall...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceJune 27, 2024· MEDLINE INDUSTRIES, LP - Northfield

Recalled Item: Medline convenience kits containing semi-rigid suction liners labeled as...

The Issue: Due to reported adverse events, Medline Industries, LP. is issuing a recall...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceJune 27, 2024· MEDLINE INDUSTRIES, LP - Northfield

Recalled Item: Medline convenience kits containing semi-rigid suction liners labeled as...

The Issue: Due to reported adverse events, Medline Industries, LP. is issuing a recall...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceJune 27, 2024· MEDLINE INDUSTRIES, LP - Northfield

Recalled Item: Medline convenience kits containing semi-rigid suction liners labeled as...

The Issue: Due to reported adverse events, Medline Industries, LP. is issuing a recall...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceJune 27, 2024· MEDLINE INDUSTRIES, LP - Northfield

Recalled Item: Medline convenience kits containing semi-rigid suction liners labeled as...

The Issue: Due to reported adverse events, Medline Industries, LP. is issuing a recall...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceJune 27, 2024· MEDLINE INDUSTRIES, LP - Northfield

Recalled Item: Medline convenience kits containing semi-rigid suction liners labeled as...

The Issue: Due to reported adverse events, Medline Industries, LP. is issuing a recall...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceJune 27, 2024· MEDLINE INDUSTRIES, LP - Northfield

Recalled Item: Medline convenience kits containing semi-rigid suction liners labeled as...

The Issue: Due to reported adverse events, Medline Industries, LP. is issuing a recall...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing