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. 1,741 recalls have been distributed to Delaware in the last 12 months.
Showing 40521–40540 of 48,330 recalls
Recalled Item: Aquapak 340 SW Recalled by Teleflex Medical Due to The seals of the...
The Issue: The seals of the respiratory gas humidifier adaptor packaging may be creased...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Aqua 540 SW Recalled by Teleflex Medical Due to The seals of the adaptor...
The Issue: The seals of the adaptor packaging may be creased which may potentially...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Aquapak SW/EAU Sterile Recalled by Teleflex Medical Due to The seals of the...
The Issue: The seals of the adaptor packaging may be creased which may potentially...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Artis zee and Artis zeego systems. x-ray Recalled by Siemens Medical...
The Issue: There is a potential problem with Artis zee and Artis zeego systems running...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: UltraStream Chronic Hemodialysis Catheter Standard Kit Recalled by Argon...
The Issue: UltraStream Chronic Hemodialysis Catheter may develop cracks on the red...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Aquapak 640 SW Recalled by Teleflex Medical Due to The seals of the adaptor...
The Issue: The seals of the adaptor packaging may be creased which may potentially...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: DMI Duro-Med Industries Rollator Transport Chair Recalled by Briggs Medical...
The Issue: There have been 5 customer reports of a 501-1018 series DMI Rollator...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Kirkland Signature Coarse Ground Malabar Pepper Recalled by Olde Thompson,...
The Issue: Olde Thompson is recalling Kirkland Signature Coarse Ground Malabar Black...
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Ferrous Gluconate Tablets Recalled by National Vitamin Co Inc Due to Mislabeling
The Issue: National Vitamin is recalling Nature's Blend Ferrous Gluconate Tablets...
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: ROSA Surgical Device 2.5.8 It is intended to be used Recalled by Zimmer...
The Issue: Software corrections reactivating the cooperative endoscopy mode.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Stride Femoral Component Size 2 Recalled by Blue Belt Technologies MN Due to...
The Issue: Mislabeled. Packages labeled PFSI-00053, Right Lateral/Left Medial contains...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Model Number(s): PB840 Ventilator (4-840120DIUU-XX). The product is a...
The Issue: In the case of a loss of GUI display due to a Backlight Inverter PCBA...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Stride Femoral Component Size 2 Recalled by Blue Belt Technologies MN Due to...
The Issue: Mislabeled. Packages labeled PFSI-00053, Right Lateral/Left Medial contains...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: InTouch Critical Care Bed Recalled by Stryker Medical Division of Stryker...
The Issue: Stryker has received complaints from the field alleging instances where the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ACL TOP 700 CTS Recalled by Instrumentation Laboratory Co. Due to Potential...
The Issue: Potential for sample misidentification.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: eye-pak 7407 Tray Support Cover Recalled by Alcon Research, Ltd. Due to The...
The Issue: The peel pouches of the Tray Support Covers may be insufficiently sealed so...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Puritan Bennett 840 Ventilator (4-840120DIUU-XX) The PB840 Ventilator System...
The Issue: Covidien is conducting a medical device field correction for specific...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: RECLAIM Taper Protector Sleeve. RECLAIM Revision Hip System Orthopedic...
The Issue: The product can be difficult to remove from the Distal Stem both out of the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: RECLAIM DISTAL TAPERED Distal Stem Recalled by DePuy Orthopaedics, Inc. Due...
The Issue: The product can be difficult to remove from the Distal Stem both out of the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ACL TOP 500 CTS Recalled by Instrumentation Laboratory Co. Due to Potential...
The Issue: Potential for sample misidentification.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.