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. 2,384 recalls have been distributed to Nebraska in the last 12 months.

49,150 total recalls
2,384 in last 12 months

Showing 4062140640 of 49,150 recalls

Medical DeviceSeptember 5, 2014· Zimmer Biomet, Inc.

Recalled Item: ROSA Surgical Device 2.5.8 ROSA Surgical Device is a computer-controlled...

The Issue: The software issue described was corrected in the modification to the...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 5, 2014· GE Healthcare, LLC

Recalled Item: GE Healthcare Precision 500D Recalled by GE Healthcare, LLC Due to GE...

The Issue: GE Healthcare has become aware of a potential safety issue involving missing...

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

Class II — Potential Health HazardOngoing
DrugSeptember 4, 2014· Hospira Inc.

Recalled Item: Bupivacaine HCl Inj. Recalled by Hospira Inc. Due to Presence of Particulate...

The Issue: Presence of Particulate Matter: A confirmed customer complaint reported the...

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

Class II — Potential Health HazardOngoing
Refund
Medical DeviceSeptember 4, 2014· Midmark Corp dba Progeny Inc

Recalled Item: Vantage Panoramic X-Ray System used to perform dental and orthodontic...

The Issue: Failure of the primary collimator may result in unintentional movement of...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 4, 2014· Teleflex Medical

Recalled Item: Rusch Recalled by Teleflex Medical Due to Misbranding: Although the product...

The Issue: Misbranding: Although the product labeling identifies the catheters as...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 3, 2014· Teleflex Medical

Recalled Item: Aqauapak 728 SW Recalled by Teleflex Medical Due to Possibility that the...

The Issue: Possibility that the nebulizer adaptor packaging may have open or weak seals...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 3, 2014· Teleflex Medical

Recalled Item: Aquapak Adaptor Recalled by Teleflex Medical Due to Possibility that the...

The Issue: Possibility that the nebulizer adaptor packaging may have open or weak seals...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 2, 2014· Aerogen Ltd.

Recalled Item: The Aeroneb Professional Nebulizer System is a portable medical device...

The Issue: Aerogen has received a small number of complaints in relation to the main...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 2, 2014· Aerogen Ltd.

Recalled Item: The Aeroneb Professional Nebulizer System is a portable medical device...

The Issue: Aerogen has received a small number of complaints in relation to the main...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 2, 2014· Aerogen Ltd.

Recalled Item: The Aeroneb Professional Nebulizer System is a portable medical device...

The Issue: Aerogen has received a small number of complaints in relation to the main...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 2, 2014· Aerogen Ltd.

Recalled Item: The Aeroneb Professional Nebulizer System is a portable medical device...

The Issue: Aerogen has received a small number of complaints in relation to the main...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 2, 2014· Siemens Medical Solutions USA, Inc

Recalled Item: Siemens AXIOM Luminos dRF Max systems The Axiom Luminos dRF Recalled by...

The Issue: Two malfunctions posing potential risk to patients were identified with...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 2, 2014· Siemens Medical Solutions USA, Inc

Recalled Item: Siemens Luminos Agile Max system The Luminos Agile is intended Recalled by...

The Issue: Two malfunctions posing potential risk to patients were identified with...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 2, 2014· Siemens Medical Solutions USA, Inc

Recalled Item: Siemens Uroskop Omnia Max system The Uroskop Omnia is a Recalled by Siemens...

The Issue: Two malfunctions posing potential risk to patients were identified with...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 2, 2014· Siemens Medical Solutions USA, Inc

Recalled Item: Siemens Ysio Max system The Ysio Max is a radiographic system used in...

The Issue: Two malfunctions posing potential risk to patients were identified with...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 2, 2014· Synthes, Inc.

Recalled Item: DePuy Synthes TI Vectra Plates: TI Vectra-One" Plate 2 Level Recalled by...

The Issue: DePuy Synthes is initiating a voluntary medical device recall of certain...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 1, 2014· Arjo Hospital Equipment AB

Recalled Item: Pressure IQ Evolve Mattress Recalled by Arjo Hospital Equipment AB Due to...

The Issue: The firm received complaints regarding multiple mattresses were showing...

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

Class II — Potential Health HazardOngoing
FoodAugust 29, 2014· Michael Foods, Inc.

Recalled Item: Papetti's Table Ready pre-cooked scrambled eggs. Keep 33 Recalled by Michael...

The Issue: Product may be contaminated with spoilage microorganism.

Recommended Action: Do not consume. Return to store for a refund or discard.

Class II — Potential Health HazardOngoing
Refund
FoodAugust 29, 2014· Michael Foods, Inc.

Recalled Item: Papetti's Table Ready pre-cooked scrambled eggs with butter flavor. Recalled...

The Issue: Product may be contaminated with spoilage microorganism.

Recommended Action: Do not consume. Return to store for a refund or discard.

Class II — Potential Health HazardOngoing
Refund
FoodAugust 29, 2014· Kraft Heinz Foods

Recalled Item: Individually 2/3 oz. slices of American cheese product individually wrapped...

The Issue: Kraft Foods Group is voluntarily recalling 7,691 cases of select varieties...

Recommended Action: Do not consume. Return to store for a refund or discard.

Class III — Low RiskOngoing
Refund