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. 2,567 recalls have been distributed to District of Columbia in the last 12 months.
Showing 14081–14100 of 27,451 recalls
Recalled Item: Vacuum Unit for CATSmart Vacuum Pump. Fresenius CATSmart (Continuous...
The Issue: The optional Vacuum Unit may stop working and display the failure message...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Infinix DP- i(Infinix-8000F) CAT-870B Catheterization Table (Titling) -...
The Issue: Table tilts without operator involvement as a result of liquid spilling into...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Cardiohelp Emergency Drive Recalled by Maquet Cardiovascular Us Sales, Llc...
The Issue: Upon servicing the gearwheel in the Emergency Drive the gearwheel may have...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Infinity Delta Family patient monitors The Infinity Delta Series...
The Issue: The firm is recalling their Delta family of patient monitors software due to...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Omega Systems These devices are intended to be used in Recalled by Draegar...
The Issue: The firm is recalling their Delta family of patient monitors software due to...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Uroskop Omnia Max -fluoroscopic X-ray system Model # 10762473 Uroskop...
The Issue: The swivel arm holding the monitors may become dislodged from the carrying arm.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Uroskop Omnia -fluoroscopic X-ray system Model # 10094910 The Uroskop...
The Issue: The swivel arm holding the monitors may become dislodged from the carrying arm.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Cordis Vista Brite Tip & Androit Guiding Catheters Product Usage: Recalled...
The Issue: Frayed pieces of the mounting card being inside the primary packaging.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Medica Wash1-Wash solution used prior to Lipase assay on the Recalled by...
The Issue: Wash1 solution is ineffective in cleaning dispensing probe of TRIG and LDL...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: LW Scientific ZIP IQ PCV Centrifuge Recalled by LW Scientific, Inc. Due to...
The Issue: The clear, plastic, polycarbonate hematocrit rotor may break apart during...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: LW Scientific ZIP IQ Combo Centrifuge Recalled by LW Scientific, Inc. Due to...
The Issue: The clear, plastic, polycarbonate hematocrit rotor may break apart during...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: LW Scientific ZIP IQ Combo Centrifuge Recalled by LW Scientific, Inc. Due to...
The Issue: The clear, plastic, polycarbonate hematocrit rotor may break apart during...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Abbott ARCHITECT Estradiol Reagent Kit - Product Usage: The ARCHITECT...
The Issue: Patient results may be falsely elevated. This patient impact only applies to...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Abbott Alinity i Estradiol Reagent Kit - Product Usage: Alinity Recalled by...
The Issue: Patient results may be falsely elevated. This patient impact only applies to...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Plain and Chromic Gut Absorbable Surgical Sutures Recalled by CP Medical Inc...
The Issue: Potential compromise of product sterility after routine monitoring for...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: US Endoscopy Padlock Clip defect closure system The Recalled by US Endoscopy...
The Issue: Potential esophageal laceration during a patient procedure
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: NexGenTrabecular Metal Tibial Half Block Augment Recalled by Zimmer...
The Issue: Potentially comingled, resulting in the product in the box potentially not...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: NexGenTrabecular Metal Tibial Half Block Augment Recalled by Zimmer...
The Issue: Potentially comingled, resulting in the product in the box potentially not...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Cook Transseptal Needle Recalled by Cook Inc. Due to The products were...
The Issue: The products were manufactured without a back bevel on the needle tip. This...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Semi-Rigid Suction Canister Recalled by Medline Industries Inc Due to...
The Issue: Potential for the Semi-Rigid canister lid to fragment during use.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.