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. 2,485 recalls have been distributed to District of Columbia in the last 12 months.
Showing 19401–19420 of 27,451 recalls
Recalled Item: Musculoskeletal Transplant Foundation Recalled by Musculoskeletal Transplant...
The Issue: AFT Diverted Tubes are being recalled due to a customer complaint involving...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Draeger D-Vapor/ D-Vapor 3000 Vaporizers with Baxter Desflurane Agent and...
The Issue: Operators noticed unwanted release of evaporating anesthetic agent at the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Acorn 130 Stairlift Recalled by Acorn Stairlifts, Inc Due to The design of...
The Issue: The design of the seats did not consistently have the adequate strength...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Surgical Table Cushion (HybriGel Pads) HybrGel Pads are an optional Recalled...
The Issue: The Surgical Table Cushion (HybriGel Pads) could potentially contain staples...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: The VITROS¿ Chemistry Products Calibrator Kit 31 Recalled by Ortho-Clinical...
The Issue: There is an incorrect value (data/calibration mathematics) on ADDs. This...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Radionuclide Radiation Therapy System Product The product is a teletherapy...
The Issue: The latches of the frame adapter can be locked even if the locating pins of...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: 3.2 mm three-fluted Radiolucent Drill Bit/Needle Point/145 mm Sterile...
The Issue: The sterile packaging may be compromised. A protective cap is to be secured...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: 3.2 mm Three-fluted drill bit Recalled by Synthes (USA) Products LLC Due to...
The Issue: The sterile packaging may be compromised. A protective cap is to be secured...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Volt Resistance Heated Slipper Black (All sizes) Deep penetrating heat...
The Issue: During an FDA inspection it was found that the firm claims unapproved...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Aprima Access Nonvascular Introducer Set Accessories Recalled by Cook Inc....
The Issue: Increase in reports of polymer degradation of the catheter tip, resulting in...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Beacon Tip Royal Flush Plus High-Flow Catheter Catheter Recalled by Cook...
The Issue: Increase in reports of polymer degradation of the catheter tip, resulting in...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Volt Resistance Heated Lower Back Garment Deep penetrating heat garment...
The Issue: During an FDA inspection it was found that the firm claims unapproved...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Shuttle Select Slip-Cath Catheter Recalled by Cook Inc. Due to Increase in...
The Issue: Increase in reports of polymer degradation of the catheter tip, resulting in...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: CARESTREAM Image Suite V4 Recalled by Carestream Health Inc Due to...
The Issue: Carestream Health received a complaint related to CARESTREAM Image Suite 4...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Volt Resistance Heated Therapy Knee Wrap Deep penetrating heat garment...
The Issue: During an FDA inspection it was found that the firm claims unapproved...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Volt Resistance Heated Slipper (All sizes) Deep penetrating heat garment...
The Issue: During an FDA inspection it was found that the firm claims unapproved...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: GE Healthcare Recalled by GE Medical Systems, LLC Due to Potential...
The Issue: Potential non-recoverable loss of image acquisition. The affected Discovery...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: TM MONO TIB STR GRN SZ 5 - 00588606510 TM Recalled by Zimmer Trabecular...
The Issue: Zimmer Biomet is initiating a recall of specific lots of foil pouched,...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Transluminal Biliary Biopsy Forceps Set Forceps Recalled by Cook Inc. Due to...
The Issue: Increase in reports of polymer degradation of the catheter tip, resulting in...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: REV. SHELL LINER 0D 28X48 00700504828 REV. SHELL LINER 10D Recalled by...
The Issue: Zimmer Biomet is initiating a recall of specific lots of foil pouched,...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.