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. 2,400 recalls have been distributed to Nebraska in the last 12 months.
Showing 37061–37080 of 49,150 recalls
Recalled Item: METHYLFOLATE Injection Recalled by Life Science Pharmacy Inc Due to...
The Issue: Penicillin Cross Contamination: potentially contaminated with penicillin
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Carb-O-Philic 40 Cream Recalled by Geritrex Corp Due to CGMP Deviation: Poor...
The Issue: CGMP Deviation: Poor container closure of the bulk storage container
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Philips HeartStart XL+ Defibrillator/Monitor Product Usage: The HeartStart...
The Issue: Multiple software and hardware issues with device that can affect its function.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Cochlear Nucleus Sterile Silicone Template Product Usage: The Cochlear ...
The Issue: Cochlear Americas is recalling Nucleus Sterile Silicone Template...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Merit Medical Prelude Pro Sheath Introducter Recalled by Merit Medical...
The Issue: Some of these introducer sheaths were packaged with a 0.035 inch dilator,...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Panoramic X-ray Model PC-1000 The PC-1000 will enable the user Recalled by...
The Issue: Jackscrew nut part failure potentially leading to device malfunction and...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: SOMATOM Emotion 6 Recalled by Siemens Medical Solutions USA, Inc Due to A...
The Issue: A potential safety issue involving two (2) broken screws and one (1) bowed,...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: APEX INTERFACE Hemi 54X and Flared 56X Recalled by Omnilife Science Inc. Due...
The Issue: The device may have improper screw hole placement due to inaccurate location...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Volcano PV .035 Catheter: Part number: 88901 Recalled by Volcano Corporation...
The Issue: During a relabeling procedure at the manufacturing facility, the products...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Prestige Plus 185cm J-Tip: Part number: 9185J Recalled by Volcano...
The Issue: During a relabeling procedure at the manufacturing facility, the products...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: SOMATOM Emotion 16 Recalled by Siemens Medical Solutions USA, Inc Due to A...
The Issue: A potential safety issue involving two (2) broken screws and one (1) bowed,...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Rifampin for Injection Recalled by Fresenius Kabi USA, LLC Due to Failed...
The Issue: Failed Impurities/Degradation Specifications; out-of-specification for...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Lutera (0.1 mg levonorgestrel and 0.02 mg ethinyl estradiol tablets USP)...
The Issue: Labeling: Incorrect or Missing Package Insert; Product is being recalled...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Dr Blue Pain Relieving Gel Recalled by Indiana Botanic Gardens, Inc Due to...
The Issue: Superpotent Drug: Product may not be uniformly blended resulting in...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: - Santa Barbara Royal Smoked Salmon 4oz. D-Cut Products are Recalled by The...
The Issue: The Santa Barbara Smokehouse, Inc. is recalling fresh and frozen cold smoked...
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: - Coastal Harbor Oak & Beechwood Smoked Salmon Sliced Side Recalled by The...
The Issue: The Santa Barbara Smokehouse, Inc. is recalling fresh and frozen cold smoked...
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: - Channel Island Atlantic Smoked Salmon Sliced Side - North Recalled by The...
The Issue: The Santa Barbara Smokehouse, Inc. is recalling fresh and frozen cold smoked...
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: - Cambridge House Mild Smoked Salmon Sliced Side - Grade Recalled by The...
The Issue: The Santa Barbara Smokehouse, Inc. is recalling fresh and frozen cold smoked...
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: - Cambridge House River Run Royal Smoked Salmon Products are Recalled by The...
The Issue: The Santa Barbara Smokehouse, Inc. is recalling fresh and frozen cold smoked...
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: - Wild River Pacific Smoked Salmon 4oz. D-Cut Products are Recalled by The...
The Issue: The Santa Barbara Smokehouse, Inc. is recalling fresh and frozen cold smoked...
Recommended Action: Do not consume. Return to store for a refund or discard.