Product Recalls in Nebraska

Product recalls affecting Nebraska — including food, drugs, consumer products, medical devices, and vehicles distributed to Nebraska. RecallDetector monitors distribution data from the FDA, USDA, CPSC, and NHTSA to show you which recalls are relevant to your area. 2,630 recalls have been distributed to Nebraska in the last 12 months.

49,150 total recalls
2,630 in last 12 months

Showing 51015120 of 49,150 recalls

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
DrugJune 28, 2024· Glenmark Pharmaceuticals Inc., USA

Recalled Item: Pravastatin Sodium Tablets Recalled by Glenmark Pharmaceuticals Inc., USA...

The Issue: Failed Dissolution Specifications: results below specifications

Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.

Class II — Potential Health HazardOngoing
Refund
DrugJune 28, 2024· Teva Pharmaceuticals USA, Inc

Recalled Item: Fludrocortisone Acetate Tablets Recalled by Teva Pharmaceuticals USA, Inc...

The Issue: Failed Impurities/Degradation Specifications: Product is being recalled due...

Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.

Class II — Potential Health HazardOngoing
Refund
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 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 27, 2024· LINK BIO CORP

Recalled Item: LINK SymphoKnee Patella Sizing Template Recalled by LINK BIO CORP Due to The...

The Issue: The LinkSymphoKnee Patella Sizing Template was incorrectly labeled. The...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 27, 2024· Medivance Inc.

Recalled Item: Arctic Sun Temperature Management Systems Recalled by Medivance Inc. Due to...

The Issue: If temperature management system fails to reach correct target water...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 27, 2024· Boston Scientific Corporation

Recalled Item: Capio SLIM Suture Capturing Device Recalled by Boston Scientific Corporation...

The Issue: Some lots of Capio SLIM do not consistently catch the suture after...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 27, 2024· Boston Scientific Corporation

Recalled Item: Capio SLIM Suture Capturing Device Recalled by Boston Scientific Corporation...

The Issue: Some lots of Capio SLIM do not consistently catch the suture after...

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: 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