Product Recalls in Delaware
Product recalls affecting Delaware — including food, drugs, consumer products, medical devices, and vehicles distributed to Delaware. RecallDetector monitors distribution data from the FDA, USDA, CPSC, and NHTSA to show you which recalls are relevant to your area. 1,069 recalls have been distributed to Delaware in the last 12 months.
Showing 7621–7640 of 48,330 recalls
Recalled Item: LIFEPAK 15 Recalled by Physio-Control, Inc. Due to Their is a potential for...
The Issue: Their is a potential for battery pins to become loose within the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: LIFEPAK 15 Recalled by Physio-Control, Inc. Due to Their is a potential for...
The Issue: Their is a potential for battery pins to become loose within the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: IRON assay Recalled by Sentinel CH SpA Due to A high recovery of Iron assay...
The Issue: A high recovery of Iron assay has been observed at some customer sites....
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: LIFEPAK 15 Recalled by Physio-Control, Inc. Due to Their is a potential for...
The Issue: Their is a potential for battery pins to become loose within the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ION* Sinus Support Nasal Spray Recalled by Biomic Sciences, LLC dba ION...
The Issue: Microbial contamination of Non-Sterile Products
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: ION*Sinus Spray Recalled by Biomic Sciences, LLC dba ION Intelligence of...
The Issue: Microbial contamination of Non-Sterile Products
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Restore Sinus Spray Recalled by Biomic Sciences, LLC dba ION Intelligence of...
The Issue: Microbial contamination of Non-Sterile Products
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Triamcinolone Acetonide Injectable Suspension Recalled by Eugia US LLC Due...
The Issue: Presence of Particulate Matter: A product complaint of a piece of glass was...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Gynazole-1 Recalled by Padagis US LLC Due to Incorrect Product Formulation:...
The Issue: Incorrect Product Formulation: Hydrophilic Colloidal Silica was used to...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Organic Protein & 50 Superfoods Protein Powder with Probiotic - Chocolate...
The Issue: Undeclared allergen; sesame
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: TRACHEAL INTUBATION FIBERSCOPE OLYMPUS LF-GP Recalled by Olympus Corporation...
The Issue: Fiberscopes do not have adequate data to support that the suction flow rate...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: JOURNEY II BCS ARTICULAR INSERT Recalled by Smith & Nephew, Inc. Due to The...
The Issue: The JRNY II BCS XLPE ART ISRT SZ 5-6 LT 10MM was laser etched, labeled and...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: JOURNEY II BCS CONSTRAINED ARTICULAR INSERT Size 5-6 Recalled by Smith &...
The Issue: The JRNY II BCS XLPE ART ISRT SZ 5-6 LT 10MM was laser etched, labeled and...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: EXALT Model D Single-Use Duodenoscope Recalled by Boston Scientific...
The Issue: Poor image quality due to fluid ingress in the lens.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: EXALT Model D Single-Use Duodenoscope: Outer box UPN# M00542420 & Recalled...
The Issue: Poor image quality due to fluid ingress in the lens.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: StealthStation S8 Application version 2.0 and 2.0.1 (Part 9735762) The...
The Issue: Due to a software anomaly which potentially could result in the surgical...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ALLERGAN UNIVERSAL FILL KIT Recalled by B. Braun Medical, Inc. Due to...
The Issue: Devices may leak as a result of a manufacturing issue. Leakage may result in...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: 30 ML 2PORT BURETTE ASSEMBLY Recalled by B. Braun Medical, Inc. Due to...
The Issue: Devices may leak as a result of a manufacturing issue. Leakage may result in...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: THERASPHERE ADMIN SET Recalled by B. Braun Medical, Inc. Due to Devices may...
The Issue: Devices may leak as a result of a manufacturing issue. Leakage may result in...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: AMO ADMINISTRATION SET Recalled by B. Braun Medical, Inc. Due to Devices may...
The Issue: Devices may leak as a result of a manufacturing issue. Leakage may result in...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.