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.

48,330 total recalls
1,069 in last 12 months

Showing 7661–7680 of 48,330 recalls

Medical DeviceSeptember 25, 2023· Aizu Olympus Co., Ltd.

Recalled Item: Cystonephroscope-endoscopic diagnosis and treatment within the bladder...

The Issue: Channel air drying process was not validated, and that a small percentage of...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 25, 2023· Aizu Olympus Co., Ltd.

Recalled Item: Transnasal esophagovideoscope-For endoscopy and endoscopic surgery within...

The Issue: Channel air drying process was not validated, and that a small percentage of...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 25, 2023· Securitas Healthcare LLC

Recalled Item: Arial Water Resistant Pendant with Wristband Recalled by Securitas...

The Issue: Premature battery depletion presents a risk that alarms will not be received...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 25, 2023· Aizu Olympus Co., Ltd.

Recalled Item: Ureteralscope- for endoscopic diagnosis and treatment within the ureter...

The Issue: Channel air drying process was not validated, and that a small percentage of...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 25, 2023· Aizu Olympus Co., Ltd.

Recalled Item: Bronchoscope - Ultrasonic: endoscopic real-time ultrasonic imaging Recalled...

The Issue: Channel air drying process was not validated, and that a small percentage of...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 25, 2023· Aizu Olympus Co., Ltd.

Recalled Item: Colonoscope-indicated for use within the lower digestive tract (including...

The Issue: Channel air drying process was not validated, and that a small percentage of...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 25, 2023· Aizu Olympus Co., Ltd.

Recalled Item: Rhinolaryngoscope-for endoscopic diagnosis and treatment within the nasal...

The Issue: Channel air drying process was not validated, and that a small percentage of...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 25, 2023· Aizu Olympus Co., Ltd.

Recalled Item: Bronchoscope-for endoscopy and endoscopic surgery within the airways and...

The Issue: Channel air drying process was not validated, and that a small percentage of...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 25, 2023· Securitas Healthcare LLC

Recalled Item: Arial Water Resistant Pendant with Neck Lanyard Recalled by Securitas...

The Issue: Premature battery depletion presents a risk that alarms will not be received...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 25, 2023· Aizu Olympus Co., Ltd.

Recalled Item: Choleodochoscope. Model Numbers: CHF-BP30 Recalled by Aizu Olympus Co., Ltd....

The Issue: Channel air drying process was not validated, and that a small percentage of...

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

Class III — Low RiskOngoing
Medical DeviceSeptember 25, 2023· Aizu Olympus Co., Ltd.

Recalled Item: Gastroscope-endoscopic ultrasound (EUS) guided fine needle aspiration (FNA)...

The Issue: Channel air drying process was not validated, and that a small percentage of...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 25, 2023· Aizu Olympus Co., Ltd.

Recalled Item: Tracheal fiberscope-airway management Recalled by Aizu Olympus Co., Ltd. Due...

The Issue: Channel air drying process was not validated, and that a small percentage of...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 25, 2023· Aizu Olympus Co., Ltd.

Recalled Item: Signmoidovideoscope-For endoscopy and endoscopic surgery within the lower...

The Issue: Channel air drying process was not validated, and that a small percentage of...

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

Class II — Potential Health HazardOngoing
FoodSeptember 25, 2023· Penzeys, Ltd.

Recalled Item: Penzeys Brady Street Cheese Sprinkle. Item 20756. net wt 2.2 Recalled by...

The Issue: Brady Street Cheese Sprinkle may contain sesame.

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

Class II — Potential Health HazardOngoing
Refund
DrugSeptember 25, 2023· Scynexis, Inc.

Recalled Item: BREXAFEMME (Ibrexafungerp) tablets 150 mg Recalled by Scynexis, Inc. Due to...

The Issue: Cross Contamination with Other Products: Potential cross-contamination of...

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

Class I — Serious Health HazardOngoing
Refund
Medical DeviceSeptember 23, 2023· Townsend Design

Recalled Item: SPRYSTEP VECTOR KAFO Recalled by Townsend Design Due to Due to potential air...

The Issue: Due to potential air pockets between layers of material, their is the...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 23, 2023· Townsend Design

Recalled Item: CUSTOM SPRYSTEP Recalled by Townsend Design Due to Due to potential air...

The Issue: Due to potential air pockets between layers of material, their is the...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 23, 2023· Townsend Design

Recalled Item: SPRYSTEP VECTOR Recalled by Townsend Design Due to Due to potential air...

The Issue: Due to potential air pockets between layers of material, their is the...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 22, 2023· Musculoskeletal Transplant Foundation, Inc.

Recalled Item: DBX Demineralized Bone Matrix Putty 10cc-Indicated for treatment of...

The Issue: Units are labeled as 10cc; however the units have a fill volume of 1cc...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 22, 2023· Olympus Corporation of the Americas

Recalled Item: Olympus High-Flow Insufflation Unit Recalled by Olympus Corporation of the...

The Issue: There have been reports of patients suffering arrhythmias, reported as short...

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

Class I — Serious Health HazardOngoing