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. 2,656 recalls have been distributed to District of Columbia in the last 12 months.
Showing 641–660 of 47,654 recalls
Recalled Item: Brand name: AGFA Digital Radiography X- Ray system DR 800 Recalled by AGFA...
The Issue: It is possible to exceed the maximum allowed Air Kerma rate (AKR) of...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Brand Name: Molift Product Name: Molift 2-point sling bars (Accessory...
The Issue: A customer experienced that during assembly and load testing of the device,...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Brand Name: Molift Product Name: Molift Mover 205 Model/Catalog Number:...
The Issue: A customer experienced that during assembly and load testing of the device,...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Brand Name: Molift Product Name: Molift 4-point sling bars (Accessory...
The Issue: A customer experienced that during assembly and load testing of the device,...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Sheathes3D Seamless Viral Barrier Recalled by Sheathing Technologies Inc Due...
The Issue: Vaginal/rectal ultrasound probe covers with a viral barrier may have product...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: The Pressio 2 ICP Monitoring System Recalled by Sophysa Due to Customer...
The Issue: Customer complaints of Pressio monitor rebooting.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Brand Name: Molift Product Name: Molift Mover 300 Model/Catalog Numbers:...
The Issue: A customer experienced that during assembly and load testing of the device,...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Brand Name: ShockPulse-SE Lithotripsy System Product Name: ShockPulse-SE...
The Issue: Ongoing investigations identified additional instances of the device...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Cinacalcet Hydrochloride Tablets Recalled by Cipla USA, Inc. Due to CGMP...
The Issue: CGMP Deviations: the presence of a nitrosamine impurity,...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Cinacalcet Hydrochloride Tablets Recalled by Cipla USA, Inc. Due to CGMP...
The Issue: CGMP Deviations: the presence of a nitrosamine impurity,...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: GE Healthcare Carestation anesthesia system Recalled by GE Medical Systems...
The Issue: Potential unexpected shutdown of Carestation 600 and 700 Series Anesthesia...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: GE Healthcare Carestation anesthesia system Recalled by GE Medical Systems...
The Issue: Potential unexpected shutdown of Carestation 600 and 700 Series Anesthesia...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Cinacalcet Hydrochloride Tablets Recalled by Cipla USA, Inc. Due to CGMP...
The Issue: CGMP Deviations: the presence of a nitrosamine impurity,...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Brand Name: ShockPulse-SE Lithotripsy System SPL-SR Product Name:...
The Issue: Ongoing investigations identified additional instances of the device...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Brand Name: ShockPulse-SE Lithotripsy System SPL-S Product Name:...
The Issue: Ongoing investigations identified additional instances of the device...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: GE Healthcare Carestation anesthesia system Power Management Board (PMB)...
The Issue: Potential unexpected shutdown of Carestation 600 and 700 Series Anesthesia...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: SCISSORS Recalled by Medline Industries, LP Due to The items may have weak...
The Issue: The items may have weak packaging seals that may result in a breach of...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: FORCEP Recalled by Medline Industries, LP Due to The items may have weak...
The Issue: The items may have weak packaging seals that may result in a breach of...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Alinity ci-series System Control Module (SCM) Recalled by Abbott...
The Issue: Abbott Laboratories is recalling their Alinity ci-series System Control...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Walgreens Saline Nasal Spray WITH XYLITOL Recalled by Medical Products...
The Issue: Microbial contamination of a non-sterile product - microorganism found to be...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.