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. 891 recalls have been distributed to District of Columbia in the last 12 months.
Showing 46621–46640 of 47,654 recalls
Recalled Item: Bayonet Forceps 7.-1/8 (181.0mm) 0.75mm Non-Insulated Tips Recalled by PSC...
The Issue: Firm officials reported to CIN-DO that for this device, in the labeling on...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: CIDEX OPA Recalled by Advanced Sterilization Products Due to The recall was...
The Issue: The recall was initiated because Advanced Sterilization Products has...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Sysmex XE-2100 Automated Hematology System Recalled by Sysmex America, Inc....
The Issue: There is a variation of reticulocyte counts between XE Series (XE-2100,...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: CARDIOGEN-82 (Rubidium Rb 82 Generator) Recalled by Bracco Diagnostics Inc...
The Issue: GMP deviation; Sr-82 levels exceeded alert limit specification
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Leukine sargramostim 5 x 500 mcg/mL vial Recalled by Bayer HealthCare...
The Issue: Impurities/Degradation Products: A confirmed out of specification result for...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Universal Spinal System Lamina Hooks Synthes Medium TI Lamina Hook Recalled...
The Issue: USS Lamina Hooks, Medium, Right are being recalled because the hooks are...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ARCHITECT CA 19-9XR Reagent Kit Recalled by Abbott Laboratories Due to The...
The Issue: The six ARCHITECT CA 19-9XR reagent lots are demonstrating a shift up in...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Adult Divided Cannula end tidal C)2 sampling w/male luer-lock connector. 7...
The Issue: A complaint was received, and later verified, that product labeled as...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Polar Whole Boiled Oysters Recalled by Milky Way Intl Trading Corp Due to MW...
The Issue: MW Polar is recalling Polar Whole Boiled Oysters from Korea because the...
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Canned oysters. Crown Prince Natural Smoked Oysters with Chili Pepper...
The Issue: The product has been prepared, packed, or held under insanitary conditions...
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Canned oysters. Crown Prince Whole Boiled Oysters Recalled by Crown Prince...
The Issue: The product has been prepared, packed, or held under insanitary conditions...
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Canned oysters. Crown Prince Whole Boiled Oysters Recalled by Crown Prince...
The Issue: The product has been prepared, packed, or held under insanitary conditions...
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Canned oysters. Crown Prince Natural Smoked Oysters in Olive Oil Recalled by...
The Issue: The product has been prepared, packed, or held under insanitary conditions...
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Hydrocodone Bitartrate & Acetaminophen Oral Solution 7.5 mg/325 mg per 15 mL...
The Issue: Impurities/Degradation Products: exceeded specification at 3 month stability...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: TRESTLE LUXE¿ Anterior Cervical Plating System Recalled by Alphatec Spine,...
The Issue: On May 9th 2012 Alphatec Spine received a complaint which reported that the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: syngo(R) Lab Data Manager and syngo(R) Lab Process Manager Recalled by...
The Issue: When using the syngo Quality Control package the system may not perform as...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: AirLife Isothermal Breathing Circuit Accessory - Infant Patient Y Connector...
The Issue: The Y adapter within the breathing circuit may spontaneously crack, causing...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: This voluntary medical device correction is related to Alcon products...
The Issue: This medical device correction is related to Alcon products that present a...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: EasyLink Informatic System is included with the Dimension Vista System....
The Issue: When using the EasyLink Quality Control Package the system may not perform...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Microbiologics 217 Osseo Avenue North Recalled by Microbiologics Inc Due to...
The Issue: Microbiologics is recalling a number of lots of KWIK-QC Gram Stain Slides....
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.