Product Recalls in District of Columbia
Product recalls affecting District of Columbia — including food, drugs, consumer products, medical devices, and vehicles distributed to District of Columbia. RecallDetector monitors distribution data from the FDA, USDA, CPSC, and NHTSA to show you which recalls are relevant to your area. 2,464 recalls have been distributed to District of Columbia in the last 12 months.
Showing 22041–22060 of 27,451 recalls
Recalled Item: Medical Device Exchange - Versaport Bladeless Trocar w/ Fixation Cannula 5mm...
The Issue: EXP did not register as a medical device establishment, list the devices...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Medical Device Exchange - KII FIOS FIRST ENTRY 5X100MM Recalled by EXP...
The Issue: EXP did not register as a medical device establishment, list the devices...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Medical Device Exchange 12x40 Airway Stent System Recalled by EXP...
The Issue: EXP did not register as a medical device establishment, list the devices...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Medical Device Exchange - Loading Unit w/ DST Series Technology 60mm - 3.5mm...
The Issue: EXP did not register as a medical device establishment, list the devices...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Medical Device Exchange - GelPort Laparoscopic System Recalled by EXP...
The Issue: EXP did not register as a medical device establishment, list the devices...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Medical Device Exchange PhysioMesh Flexible Composite Mesh 15 x 15cm...
The Issue: EXP did not register as a medical device establishment, list the devices...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: G7 Variant Elution Buffer HiS no. 1 (M) component of Recalled by Tosoh...
The Issue: The G7 Variant Elution Buffer HiS no. 1 (M) is incorrectly labeled with an...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Philips Healthcare DuraDiagnost X- Ray Recalled by Philips Medical Systems,...
The Issue: The system is designed to emit a beep upon termination of an exposure....
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: CooperSurgical PESSARY KIT-CUBE#2 Recalled by CooperSurgical, Inc. Due to...
The Issue: Incorrect size printed on the Milex Pessary Kit packaging label
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Philips Healthcare DigitalDiagnost System X-Ray Recalled by Philips Medical...
The Issue: The system is designed to emit a beep upon termination of an exposure....
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: SIEMENS SOMATOM Force with software version VA50A and /or VA50A_FP1 Recalled...
The Issue: Possibility of image artifacts during data acquisition when using Adaptive...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Terumo HX2 Temperature Management System provides temperature control of two...
The Issue: Malfunctioning mixing valve and loss of cooling and/or heating capability....
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ARROW FiberOptix Intra-Aortic Balloon Catheter Kit Recalled by Arrow...
The Issue: Outer package product label incorrectly identifies the product as FiberOptix...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Computed Tomography X-ray Systems Brilliance iCT SP. Intended to produce...
The Issue: 5 issues. Fast Get Ready incorrectly enabled during service procedures....
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Zip 8M Wound Closure Device Recalled by Zipline Medical Due to The...
The Issue: The manufacturers seal may not be present on the Nylon pouch resulting in...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Zip 16 Surgical Skin Closure Device Recalled by Zipline Medical Due to The...
The Issue: The manufacturers seal may not be present on the Nylon pouch resulting in...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Computed Tomography X-ray systems Brilliance iCT Recalled by Philips Medical...
The Issue: 5 issues. Fast Get Ready incorrectly enabled during service procedures....
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Zip 8i Surgical Skin Closure Device Recalled by Zipline Medical Due to The...
The Issue: The manufacturers seal may not be present on the Nylon pouch resulting in...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: DermaPen Pro Model Recalled by Derma Pen, LLC Due to Derma Pen initiated a...
The Issue: Derma Pen initiated a field communication for Dermapen after receiving an...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Computed Tomography X-ray Systems (Brilliance CT 64-channel w/Essence...
The Issue: Philips discovered that a software defect exists in marketed product wherein...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.