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. 1,870 recalls have been distributed to District of Columbia in the last 12 months.
Showing 12621–12640 of 27,451 recalls
Recalled Item: Japan DISP SET Recalled by Haemonetics Corporation Due to Potential to...
The Issue: Potential to develop leaks at the inner core of Cell Saver¿ 5/5+ and Cell...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: CS5/5+ Fastpacks Recalled by Haemonetics Corporation Due to Potential to...
The Issue: Potential to develop leaks at the inner core of Cell Saver¿ 5/5+ and Cell...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: CS Elite Processing Set (125 ml) Autotransfusion Device - Product Recalled...
The Issue: Potential to develop leaks at the inner core of Cell Saver¿ 5/5+ and Cell...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: High Speed Cell Saver¿5/5+ Bowl Set Autotransfusion Device - Product...
The Issue: Potential to develop leaks at the inner core of Cell Saver¿ 5/5+ and Cell...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: JAPAN CELL SAVER ELITE SET - 125ML - Product Usage: Recalled by Haemonetics...
The Issue: Potential to develop leaks at the inner core of Cell Saver¿ 5/5+ and Cell...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: JAPAN BASIC HI SPEED CS5 SET Recalled by Haemonetics Corporation Due to...
The Issue: Potential to develop leaks at the inner core of Cell Saver¿ 5/5+ and Cell...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: JAPAN LOW VOL(125ML) CS5 SET Recalled by Haemonetics Corporation Due to...
The Issue: Potential to develop leaks at the inner core of Cell Saver¿ 5/5+ and Cell...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: MicroScan WalkAway-96 plus Reconditioned Instrument Recalled by Beckman...
The Issue: WalkAway Instruments may have been assembled with the incorrect AC power...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: MicroScan WalkAway-40 plus Instrument Recalled by Beckman Coulter Inc. Due...
The Issue: WalkAway Instruments may have been assembled with the incorrect AC power...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: MicroScan WalkAway-96 plus Instrument Recalled by Beckman Coulter Inc. Due...
The Issue: WalkAway Instruments may have been assembled with the incorrect AC power...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: DxM 1040 MicroScan WalkAway Instrument Recalled by Beckman Coulter Inc. Due...
The Issue: WalkAway Instruments may have been assembled with the incorrect AC power...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: MicroScan WalkAway-40 plus Reconditioned Instrument Recalled by Beckman...
The Issue: WalkAway Instruments may have been assembled with the incorrect AC power...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: DxM 1096 MicroScan WalkAway Instrument Recalled by Beckman Coulter Inc. Due...
The Issue: WalkAway Instruments may have been assembled with the incorrect AC power...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Aequalis Ascend Flex Humeral Stem: Part Number UDI DWF601A 3700386944475...
The Issue: During shipping, it is possible for the Aequalis Ascend Flex humeral stem to...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: CapsoCAM Plus Recalled by Capso Vision, Inc. Due to Capsule Endoscopy...
The Issue: Capsule Endoscopy System: a defect present in the capsule window may be...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: BRASSELER KM166-310-35 Twist Drill Quick Connect Diameter 3.5 mm Recalled by...
The Issue: One lot of 3.5 mm twist drills were incorrectly laser etched as 2.5 mm the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: HeartStart XL+ Defibrillator/Monitor Recalled by Philips North America, LLC...
The Issue: The rotary therapy selector switch may fail, resulting in unexpected device...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: i-STAT cTnI cartridge Recalled by Abbott Point Of Care Inc. Due to i-STAT¿...
The Issue: i-STAT¿ cTnI blue cartridges may generate a higher than expected number of...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: BD Posiflush Pre-Filled Normal Saline Syringes Catalog Number: 306575...
The Issue: Limited number of syringes labeled Posiflush Experimental Product and Not...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Levo Arm Label: LEVO ARM MIZUHO OSI Recalled by Mizuho OSI Due to Due to the...
The Issue: Due to the potential for fluid ingress into the Arm which could affect the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.