Recalls distributed in Nebraska
These notices name Nebraska in the distribution list the company gave its agency. That list says where the product was shipped, not where it ended up — a recalled item can travel with a shopper, and some notices list no states at all.
2,352 stored notices name Nebraska, reported between Jun 20, 2012 and Sep 23, 2026. A further 48,100 notices were distributed nationwide, so they reach Nebraska too — those are in the archive.
Reported Dec 18, 2019
Passive Biopsy Needle Kit, UDI: 00643169030121 and 00643169702943
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Medtronic Navigation, Inc.
2 more products in this recall
FDA (openFDA device enforcement)
Reported Dec 18, 2019
P28, Titan 3-D Wedge, Evans, Large, 10 mm, sterile, REF P03-EVN-1010-S, Type: Lagrge, Size: 10mm, (01) 00889795018182,…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Paragon 28, Inc.
FDA (openFDA device enforcement)
Reported Dec 18, 2019
Natural Grocers SOYBEANS ORGANIC in 2.0 lbs (32 oz) (907 g) plastic retail bags, 9 bags/case, Packaged by Vitamin…
Low riskThis product is unlikely to cause harm, but it breaks a safety or labelling rule.Vitamin Cottage Natural Foods Market, Inc. dba Natural Grocers
FDA (openFDA food enforcement)
Reported Dec 11, 2019
Color Cuff Disposable Tourniquet Cuff, 18 inch X 3 inch, 1BLA (Single Bladder), 1PRT(Single Port) Quick Connect…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Stryker Instruments Div.
1 more product in this recall
FDA (openFDA device enforcement)
Reported Dec 4, 2019
Atellica CH 930 Analyzer
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Siemens Healthcare Diagnostics, Inc.
FDA (openFDA device enforcement)
Reported Nov 27, 2019
EZ Glide Aortic Cannula, 24 Fr. (8.0mm) x 37.6 cm (14.8") 3/8" (9.5 mm) vented connector , RX Only, Sterile EC, Made in…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Edwards Lifesciences, LLC
FDA (openFDA device enforcement)
Reported Nov 27, 2019
Tomato, Carrot, Broccoli & Snap Pea- 13 oz in clear plastic container. Brands: Crazy Fresh, Quick&Easy, or Plain Label
High riskUsing this product could cause serious injury, illness or death — stop using it now.Russ Davis Wholesale, Inc.
16 more products in this recall
FDA (openFDA food enforcement)
Reported Nov 27, 2019
Simplot simple goodness Classic Mixed Vegetables, foodservice item. There are 12/2.5 lbs. clear plastic bags per case.…
High riskUsing this product could cause serious injury, illness or death — stop using it now.Simplot-Rdo LLC
FDA (openFDA food enforcement)
Reported Nov 20, 2019
2000 Vascular with 30 Degree option
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Heritage Medical Products, Inc.
FDA (openFDA device enforcement)
Reported Nov 13, 2019
Prismaflex Control Unit, software versions below 7.21
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Baxter Healthcare Corporation
4 more products in this recall
FDA (openFDA device enforcement)
Reported Nov 13, 2019
Sweet Smiles brand Select Dark Chocolate with Orange Peel Bar in 3.5 oz. foil wrapper packaging.
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Dollar General Corporation
FDA (openFDA food enforcement)
Reported Nov 13, 2019
StemPro¿ MSC SFM CTS"
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Life Technologies Corporation
1 more product in this recall
FDA (openFDA device enforcement)
Reported Nov 13, 2019
The LivaNova VNS Therapy System, used for Vagus Nerve Stimulation (VNS), consists of an implantable VNS Therapy…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.LivaNova USA Inc.
FDA (openFDA device enforcement)
Reported Nov 13, 2019
Babi.Plus 12.5 cm H2O Pressure Relief Manifold Catalog # 2691 for use with ventilators.
High riskUsing this product could cause serious injury, illness or death — stop using it now.Teleflex-Morrisville
FDA (openFDA device enforcement)
Reported Nov 6, 2019
CardioLab/ComboLab Recording Systems
Moderate riskThis product could cause temporary or reversible health problems — stop using it.GE Healthcare, LLC
FDA (openFDA device enforcement)
Reported Nov 6, 2019
Implant Direct Scan Adapter Assembly Replant platform for the following part numbers: 6035-09PT-M (3.5mmD)/UDI :…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Implant Direct Sybron Manufacturing, LLC
FDA (openFDA device enforcement)
Reported Nov 6, 2019
Synchro2, 0.014 in x 200cm, SOFT Guidewire with Hydrophilic Coating, UPN Product No. M00326010 REF 2601, STERILE: EO -…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Stryker Neurovascular
7 more products in this recall
FDA (openFDA device enforcement)
Reported Oct 30, 2019
Sterile Co-Flex NL 3" - Product Usage: Single Use secondary wound dressing or compression wrap.
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Andover Healthcare Inc.
5 more products in this recall
FDA (openFDA device enforcement)
Reported Oct 30, 2019
EXACTAMIX Empty EVA (Ethylene Vinyl Acetate) TPN Bag with the following product code and sizes: 1. H938737, 250mL; 2.…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Baxter Healthcare Corporation
FDA (openFDA device enforcement)
Reported Oct 30, 2019
ApexPro Telemetry Server System. Also identified as Modification To: ApexPro Telemetry System and ApexPro FH Telemetry…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.GE Healthcare, LLC
FDA (openFDA device enforcement)
Reported Oct 30, 2019
The ICS CHARTR EP 200
Moderate riskThis product could cause temporary or reversible health problems — stop using it.GN Otometrics
FDA (openFDA device enforcement)
Reported Oct 30, 2019
GRIPPER Needles sold individually. Labeled as the following item descriptions: 1. NDL, GRIPPER, 22G X 1" (25MM), 12/BX;…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Smiths Medical ASD Inc.
1 more product in this recall
FDA (openFDA device enforcement)
Reported Oct 23, 2019
Infusion Pump I.V. Administration, specifically Plum Microbore Infusion Sets with Inline Filters labeled as…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.ICU Medical Inc.
21 more products in this recall
FDA (openFDA device enforcement)
Reported Oct 23, 2019
Roche Diagnostics cobas Integra Albumin Gen.2 Catalog Number: 05166861190 - Product Usage: In vitro test for the…
Low riskThis product is unlikely to cause harm, but it breaks a safety or labelling rule.Roche Diagnostics Operations, Inc.
1 more product in this recall
FDA (openFDA device enforcement)
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RecallNow is not a government agency. Every notice above was published by the FDA, USDA FSIS or CPSC and links back to its source. Browse the whole archive.