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. 2,423 recalls have been distributed to District of Columbia in the last 12 months.
Showing 36661–36680 of 47,654 recalls
Recalled Item: R3(TM) 22 MM I.D. Recalled by Smith & Nephew, Inc. Due to The R3 Constrained...
The Issue: The R3 Constrained outer liner locking groove diameter is 0.030 inches...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: syngo Workflow SLR Recalled by Siemens Medical Solutions USA, Inc Due to A...
The Issue: A potential exists for order transactions from interfaced HIS (Hospital...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: VITROS Immunodiagnostic Products Signal Reagent Recalled by ORTHO-CLINICAL...
The Issue: The Immunodiagnostic Products Signal Reagent, Lot 3082 as the reagent packs...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: D2-40 (Lymphatic Marker) Recalled by Biocare Medical, LLC Due to Firm...
The Issue: Firm discovered that incorrect Instructions for Use were shipped with one...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ONCOR Avant Garde Recalled by Siemens Medical Solutions USA, Inc Due to...
The Issue: potential safety risk of collision of the LINAC gantry with the patient or...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Cios Alpha Recalled by Siemens Medical Solutions USA, Inc Due to under...
The Issue: under certain circumstances the Cios Alpha system may freeze during a procedure.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Edwards Lifesciences IntraClude Intra-Aortic Occlusion Device Recalled by...
The Issue: Potential device damage on the strain relief near the hub area, which may...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Astral 100 ( Model No. 27001) & Astral 150 (Model No. 27003) ventilator....
The Issue: The Astral device allows clinicians to disable all alarms including those...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Swan-Ganz CCO/Sv02/CEDV/VIP Thermodilution Catheters model number 744HF75....
The Issue: The product failed to meet the internal established statistical test...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Loratadine Orally Disintegrating Tablets USP Recalled by Ohm Laboratories,...
The Issue: Superpotent Drug: Out Of Specification (OOS) result for Assay.
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Natural Creations Glucosamine MSM 90 capsules packaged in 250 cc Recalled by...
The Issue: Natural Creations is recalling Glucosamine MSM dietary supplement due to...
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Spine Wave Access Kit Recalled by Spine Wave, Inc. Due to Mislabeling
The Issue: Mislabeled outer carton: Monopolar Probe is listed as 200 x 1.5mm when it...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Navigation System II-Cart Recalled by Stryker Instruments Div. of Stryker...
The Issue: Stryker initiated a device recall of the Navigation System II-Cart, Camera...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Remel Blood Agar (TSA w/sheep blood) plate packaged Recalled by Remel Inc...
The Issue: Product may be contaminated with Listeria monocytogenes.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Synovis VASCU-GUARD Peripheral Vascular Patch in the following sizes and...
The Issue: Baxter healthcare is recalling specific product codes of Vascu-Guard...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Poco Dolce Bittersweet Chocolate: Ginger Tile Recalled by Poco Dolce...
The Issue: California Department of Public Health conducted and inspection of the firm...
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Poco Dolce Bittersweet Chocolate: Sesame Toffee Tile Recalled by Poco Dolce...
The Issue: California Department of Public Health conducted and inspection of the firm...
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Poco Dolce Bittersweet Chocolate: Burnt Caramel Tile Recalled by Poco Dolce...
The Issue: California Department of Public Health conducted and inspection of the firm...
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Poco Dolce Bittersweet Chocolate: Almond Tile Recalled by Poco Dolce...
The Issue: California Department of Public Health conducted and inspection of the firm...
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Poco Dolce Bittersweet Chocolate: Aztec Chili Tile Recalled by Poco Dolce...
The Issue: California Department of Public Health conducted and inspection of the firm...
Recommended Action: Do not consume. Return to store for a refund or discard.