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. 2,429 recalls have been distributed to District of Columbia in the last 12 months.
Showing 36001–36020 of 47,654 recalls
Recalled Item: ATTUNE CONV RP PS ARTICULATION SURFACE SZ1-9 INTENDED USE: The Recalled by...
The Issue: Potential for the Balseal, a small wire spring coil located on the post...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: OxySure Model 615 disposable replacement cartridges Recalled by Oxysure...
The Issue: Flow rate of the recalled replacement cartridges does not meet the draft FDA...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: GE Healthcare Precision 500D Classical R & F system. Recalled by GE...
The Issue: A reported incident of a monitor that fell from the suspension. A fall of a...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: PYROLA Advanced Joint Formula capsules Recalled by GC Natural Nutrition,...
The Issue: Marketed Without An Approved NDA/ANDA: Product was found to contain...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: On-X Prosthetic Heart Valve Product Usage: Indicated for the replacement...
The Issue: Incorrect product label. The type of Sewing Ring was mislabeled as being a...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: JustRight 5mm Reload Recalled by Justright Surgical, LLC Due to JustRight...
The Issue: JustRight Surgical is recalling various lots of JustRight 5mm Stapler...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: JustRight 5mm Stapler Recalled by Justright Surgical, LLC Due to JustRight...
The Issue: JustRight Surgical is recalling various lots of JustRight 5mm Stapler...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ARCHITECT c8000 System List Number 01G06-98 Product Usage: The Abbott...
The Issue: The ARCHITECT c8000 instrument contains tubing that does not meet...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: NDI Disposable Marker Spheres for Brainlab IGS (Image Guided Recalled by...
The Issue: Inadequate curing of adhesive, may cause the two halves of the spheres to...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Magnus Hybrid OR Table Column (1180.01B2) used in conjunction with Recalled...
The Issue: There is a potential issue that could result to collision between the C-arm...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Helical Blade Inserter for Trochanteric Fixation Nail-ADVANCED (TFNA)...
The Issue: The height of one of the three guiding pins of the Helical Blade Inserter...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: OXYCODONE HCl C-II Tablets Recalled by The Harvard Drug Group, LLC Due to...
The Issue: Superpotent Drug: Confirmed customer complaint of a single unit dose blister...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: NEXIUM¿ (esomeprazole magnesium) Recalled by AstraZeneca Pharmaceuticals LP...
The Issue: Presence of Foreign Tablets/Capsules: Confimed customer compliant by a...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Offset Femoral Alignment Guide Recalled by Omnilife Science Inc. Due to The...
The Issue: The markings on both versions of the OFFSET FEMORAL ALIGNMENT GUIDES are...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Offset Femoral Alignment Guide 4mm x 6¿ Recalled by Omnilife Science Inc....
The Issue: The markings on both versions of the OFFSET FEMORAL ALIGNMENT GUIDES are...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Olympus Scientific Solutions Americas Analytical X-ray System. Delta...
The Issue: Higher than published scatter around the probe head when testing some...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Nakoma-SL Anterior Cervical Plating System's Variable Single Barrel Drill...
The Issue: Inadequate interference between the screw and the plate when screw implanted...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: TRI-EST Lozenges Recalled by Life Science Pharmacy Inc Due to Penicillin...
The Issue: Penicillin Cross Contamination: potentially contaminated with penicillin
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: HYDROXOCOBALAMIN Injection Recalled by Life Science Pharmacy Inc Due to...
The Issue: Penicillin Cross Contamination: potentially contaminated with penicillin
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: BI-EST Suspensions Recalled by Life Science Pharmacy Inc Due to Penicillin...
The Issue: Penicillin Cross Contamination: potentially contaminated with penicillin
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.