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 36041–36060 of 47,654 recalls
Recalled Item: Carb-O-Philic 40 Cream Recalled by Geritrex Corp Due to CGMP Deviation: Poor...
The Issue: CGMP Deviation: Poor container closure of the bulk storage container
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Philips HeartStart XL+ Defibrillator/Monitor Product Usage: The HeartStart...
The Issue: Multiple software and hardware issues with device that can affect its function.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Cochlear Nucleus Sterile Silicone Template Product Usage: The Cochlear ...
The Issue: Cochlear Americas is recalling Nucleus Sterile Silicone Template...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Rifampin for Injection Recalled by Fresenius Kabi USA, LLC Due to Failed...
The Issue: Failed Impurities/Degradation Specifications; out-of-specification for...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Dr Blue Pain Relieving Gel Recalled by Indiana Botanic Gardens, Inc Due to...
The Issue: Superpotent Drug: Product may not be uniformly blended resulting in...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Lutera (0.1 mg levonorgestrel and 0.02 mg ethinyl estradiol tablets USP)...
The Issue: Labeling: Incorrect or Missing Package Insert; Product is being recalled...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Panoramic X-ray Model PC-1000 The PC-1000 will enable the user Recalled by...
The Issue: Jackscrew nut part failure potentially leading to device malfunction and...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: APEX INTERFACE Hemi 54X and Flared 56X Recalled by Omnilife Science Inc. Due...
The Issue: The device may have improper screw hole placement due to inaccurate location...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: SOMATOM Emotion 6 Recalled by Siemens Medical Solutions USA, Inc Due to A...
The Issue: A potential safety issue involving two (2) broken screws and one (1) bowed,...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: SOMATOM Emotion 16 Recalled by Siemens Medical Solutions USA, Inc Due to A...
The Issue: A potential safety issue involving two (2) broken screws and one (1) bowed,...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Prestige Plus 185cm J-Tip: Part number: 9185J Recalled by Volcano...
The Issue: During a relabeling procedure at the manufacturing facility, the products...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Volcano PV .035 Catheter: Part number: 88901 Recalled by Volcano Corporation...
The Issue: During a relabeling procedure at the manufacturing facility, the products...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Smart Lipo Dietary Supplement capsules Recalled by Centro Naturista Due to...
The Issue: Marketed without an approved NDA/ANDA - Product contains undeclared...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Smart Lipo Dietary Supplement capsules Recalled by Centro Naturista Due to...
The Issue: Marketed without an approved NDA/ANDA - Product contains undeclared...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Heparin Sodium and 0.9% Sodium Chloride Injection Recalled by Baxter...
The Issue: Subpotent Drug; out of specification results for heparin raw material
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Smart Lipo Dietary Supplement capsules Recalled by Centro Naturista Due to...
The Issue: Multiple dietary supplement regulation violations.
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Smith & Nephew BIRMINGHAM HIP (TM) RESURFACING FEMORAL HEAD Recalled by...
The Issue: The firm observed that the BIRMINGHAM HIP(TM) Resurfacing (BHR) System had...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Smith & Nephew BIRMINGHAM HIP (TM) RESURFACING ACETABULAR CUP W/IMPACTOR...
The Issue: The firm observed that the BIRMINGHAM HIP(TM) Resurfacing (BHR) System had...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Smith & Nephew BIRMINGHAM HIP (TM) RESURFACING DYSPLASIA CUP W/IMPACTOR...
The Issue: The firm observed that the BIRMINGHAM HIP(TM) Resurfacing (BHR) System had...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Alaris Medley LVP Frame Membrane. Intended use to hold platen Recalled by...
The Issue: Administration of inappropriate quantities of fluid can result, with the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.