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 1101–1120 of 47,654 recalls
Recalled Item: MEDLINE convenience kits labeled as: 1) HEAD AND NECK Recalled by Medline...
The Issue: Medline Industries, LP is issuing a recall for specific item(s) and lot(s)...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: MEDLINE convenience kits labeled as: 1) BASIC NEURO PACK Recalled by Medline...
The Issue: Medline Industries, LP is issuing a recall for specific item(s) and lot(s)...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Brand Name: Leksell Stereotactic System Product Name: Leksell Vantage...
The Issue: Due to increased risk that paint flakes from the engravings may separate...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: IMRIS Operating Suite Recalled by IMPRIS Imaging Inc Due to There is a...
The Issue: There is a potential safety issue associated with the magnet venting paths...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: IMRIS Operating Suite Recalled by IMPRIS Imaging Inc Due to There is a...
The Issue: There is a potential safety issue associated with the magnet venting paths...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: BD Pyxis Pro MedStation Main Recalled by CareFusion 303, Inc. Due to...
The Issue: Potential fluid ingress of anesthesia station or med station may result in...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Various models of BD Pyxis MedFlex Recalled by CareFusion 303, Inc. Due to...
The Issue: Potential fluid ingress of anesthesia station or med station may result in...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Various models of BD Pyxis Pro 7-Drawer Auxiliary Recalled by CareFusion...
The Issue: Potential fluid ingress of anesthesia station or med station may result in...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: IMRIS Operating Suite Recalled by IMPRIS Imaging Inc Due to There is a...
The Issue: There is a potential safety issue associated with the magnet venting paths...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: IMRIS Operating Suite Recalled by IMPRIS Imaging Inc Due to There is a...
The Issue: There is a potential safety issue associated with the magnet venting paths...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: All Serial Numbers/BD Pyxis CII Safe ES Tower Main Recalled by CareFusion...
The Issue: Potential fluid ingress of anesthesia station or med station may result in...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Various models of BD Pyxis Medbank: numbers: 1137-00 1145-00 Recalled by...
The Issue: Potential fluid ingress of anesthesia station or med station may result in...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Brand Name: Hemodialysis Bloodlines Product Name: STREAMLINE BLOODLINE SET...
The Issue: The potential for micro-air bubbles observed in the bloodline and...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Medline Recalled by Medline Industries, LP Due to Subpotent Drug
The Issue: Subpotent Drug
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Doxycycline Hyclate Tablets Recalled by Acella Pharmaceuticals, LLC Due to...
The Issue: Failed dissolution specifications: Stability testing found that the lot did...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: AFCO Recalled by Acuity Specialty Products, Inc. Due to cGMP deviations: The...
The Issue: cGMP deviations: The recall was initiated because required receipt testing...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Wyandotte Recalled by Acuity Specialty Products, Inc. Due to cGMP...
The Issue: cGMP deviations: The recall was initiated because required receipt testing...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Italian Parsley packaged in 24lb boxes Recalled by MAYEJ COMERCIALIZADORA S....
The Issue: pathogen Cyclospora cayetanensis
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Succinylcholine Chloride Injection Recalled by Dr. Reddy's Laboratories,...
The Issue: Out-of-Specification (OOS) result during the 6-month stability testing;...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Brand Name: AART Calf Implant Product Name: Calf Implant Model/Catalog...
The Issue: Due to manufactured products that deviated from established specifications...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.