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 48,122 notices were distributed nationwide, so they reach Nebraska too — those are in the archive.
Reported Jun 12, 2013
Comfort brand Ear-Loop Face Mask, Item #: 3100, Model Numbers: # 3100B, # 3100P, # 3100G, # 3100Y, # 3100W; Product is…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Maytex Corp.
FDA (openFDA device enforcement)
Reported Jun 5, 2013
AngioDynamics Micro Introducer Kits under the following labeling: 1) AngioDynamics 4F Standard Micro-Introducer Kit,…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Angiodynamics, Inc.
1 more product in this recall
FDA (openFDA device enforcement)
Reported May 29, 2013
Cardinal Health hCG Cassette Rapid Test, Part Number: B1077-22 (Mfg PN: 4582105026) The SP hCG Cassette Rapid Test is a…
Low riskThis product is unlikely to cause harm, but it breaks a safety or labelling rule.Alere San Diego, Inc.
FDA (openFDA device enforcement)
Reported May 29, 2013
Ref: VP1600 HD Still Capture System ConMed Linvatec . Captures, stores and transfers images generated by a medical…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Linvatec Corp. dba ConMed Linvatec
FDA (openFDA device enforcement)
Reported May 29, 2013
Brilliance CT 16-Slice Water, System Code: 728245; Brilliance CT 10-Slice Water, System Code: 728250; Brilliance CT…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Philips Medical Systems (Cleveland) Inc.
FDA (openFDA device enforcement)
Reported May 29, 2013
Progressive Medical PTFE Coated Disposable Electrosurgical Electrodes - NON-STICK CAUTERY TIP PTFE Modified Coated…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Progressive Medical Inc.
16 more products in this recall
FDA (openFDA device enforcement)
Reported May 22, 2013
AMS 800¿ Urinary Control System. The AMS 800¿ Urinary Control System is used to treat urinary incontinence due to…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.American Medical Systems, Inc.
1 more product in this recall
FDA (openFDA device enforcement)
Reported May 22, 2013
GE Healthcare Innova 2100 IQ, Innova 3100 IQ, Innova 4100 IQ, Innova 2121 IQ, Innova 3131 IQ , Innova 3100, Innova…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.GE Healthcare, LLC
FDA (openFDA device enforcement)
Reported May 22, 2013
Add a Scoop by Smoothie Essentials; Probiotic; Supports Digestive Health, dietary supplement; Net Weight: 1 lb (464g)…
Low riskThis product is unlikely to cause harm, but it breaks a safety or labelling rule.Juice Bar Solutions
FDA (openFDA food enforcement)
Reported May 15, 2013
KARL STORZ Photodynamic Diagnosis (PDD) D-Light C System, Instruction Manuals: PDD Telescopes, Tricam SL II, and PDD…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Karl Storz Endoscopy America Inc.
FDA (openFDA device enforcement)
Reported May 15, 2013
Olympus SurgMaster UES-40 electrosurgical unit ("UES-40") Product Usage: Designed for use in a medical facility under…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Olympus America Inc.
FDA (openFDA device enforcement)
Reported May 8, 2013
STERRAD CYCLESURE 24 Biological Indicator (BI) The STERRAD CYCLESURE 24 Biological Indicator (BI), is intended to be…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Advanced Sterilization Products
FDA (openFDA device enforcement)
Reported May 8, 2013
BUFFALO TRACE BOURBON FLAVORED CARAMEL SAUCE 8 oz glass jars Net Wt. 8 fl. oz./227 g, PRODUCED BY: APPLECREEK ORCHARDS…
High riskUsing this product could cause serious injury, illness or death — stop using it now.Buffalo Trace Distillery
4 more products in this recall
FDA (openFDA food enforcement)
Reported May 1, 2013
all One Active Senior Multiple Vitamin & Mineral Powder dietary supplement, 30 Day Supply, 15.9 oz. canisters
Moderate riskThis product could cause temporary or reversible health problems — stop using it.All One, Inc.
1 more product in this recall
FDA (openFDA food enforcement)
Reported May 1, 2013
NeuViz 16 Multi-Slice CT Scanner System, Part number (PN): 989605858501, Model: NeuViz 16. This is a computed X-ray,…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Philips And Neusoft Medical Systems Co., Ltd.
1 more product in this recall
FDA (openFDA device enforcement)
Reported Apr 24, 2013
EVOTECH Endoscope Cleaner & Reprocessor System, P/N 50004 Designed to automatically clean and high-level disinfect…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Advanced Sterilization Products
1 more product in this recall
FDA (openFDA device enforcement)
Reported Apr 24, 2013
Metal cans; labeled as containing 29 oz of pinto beans packed in water and salt
Moderate riskThis product could cause temporary or reversible health problems — stop using it.La Preferida Inc.
FDA (openFDA food enforcement)
Reported Apr 24, 2013
Siemens Dimension Vista(R) System Vista Drug 4 Calibrator. The device is used as an in vitro diagnostic product.
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Siemens Healthcare Diagnostics, Inc.
FDA (openFDA device enforcement)
Reported Apr 24, 2013
Siemens syngo WorkFlow SLR, Radiological Information System, Version VA31A SP1/SP2/SP3 The information system syngo(R)…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Siemens Medical Solutions USA, Inc.
FDA (openFDA device enforcement)
Reported Apr 17, 2013
Giraffe OmniBed¿ and Giraffe Incubator p/n 6600-0723-700 (rev A and B) labeled in part: ***GE Healthcare 8880 Gorman…
High riskUsing this product could cause serious injury, illness or death — stop using it now.GE Healthcare, LLC
4 more products in this recall
FDA (openFDA device enforcement)
Reported Apr 17, 2013
NewChapter Probiotic Elderberry, 90 vegetarian capsules bottle. Dietary Supplement UPC: 7-27783-00123-8
High riskUsing this product could cause serious injury, illness or death — stop using it now.New Chapter, Inc.
FDA (openFDA food enforcement)
Reported Apr 17, 2013
Dade(R) Actin(R) FSL Activated PTT Reagent. For use in the determination of the activated partial thromboplastin time…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Siemens Healthcare Diagnostics, Inc.
FDA (openFDA device enforcement)
Reported Apr 17, 2013
CO2 Incubators (General Purpose Incubator), model numbers 370, 371, 380, 381, 3307, 3308, 3310, 3311, 3540, 3541, 3542,…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Thermo Fisher Scientific (Asheville) LLC
FDA (openFDA device enforcement)
Reported Apr 17, 2013
G7 HPLC. Used as an aid in the detection and presumptive identification of abnormal hemoglobins in whole blood.
Low riskThis product is unlikely to cause harm, but it breaks a safety or labelling rule.Tosoh Bioscience Inc.
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.