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. 2,448 recalls have been distributed to District of Columbia in the last 12 months.
Showing 27281–27300 of 47,654 recalls
Recalled Item: Foot Controls impacted for the following devices: OAKWORKS¿ Medical CFPM...
The Issue: The foot control used on the OAKWORKS¿ Inc., CFPM300, CFPM301, CFPM400,...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Spectrum Central Venous Catheter Tray Minocycline/Rifampin Antibiotic...
The Issue: Central venous catheters may not fit over guide wire potentially causing...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Central Venous Catheter Set Heparin Coated Triple Lumen Polyurethane...
The Issue: Central venous catheters may not fit over guide wire potentially causing...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Central Venous Catheter Tray Triple Lumen Polyurethane Recalled by Cook Inc....
The Issue: Central venous catheters may not fit over guide wire potentially causing...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Central Venous Tray Triple Lumen Polyurethane Catheter Recalled by Cook Inc....
The Issue: Central venous catheters may not fit over guide wire potentially causing...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Central Venous Catheter Set Triple Lumen Polyurethane Recalled by Cook Inc....
The Issue: Central venous catheters may not fit over guide wire potentially causing...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Friendly Farms Key Lime Crunch Tilts Greek Lowfat Yogurt Recalled by...
The Issue: Recalling Friendly Farms Key Lime Crunch Tilts because it may contain...
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: 85" (216 cm) Y-Type Blood Set w/170 Micron Filter Recalled by ICU Medical,...
The Issue: Some devices were labeled as Does not contain DEHP even though the product...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: 80" (203 cm) 20 Drop Y-Type Blood Set w/200 Micron Filter Recalled by ICU...
The Issue: Some devices were labeled as Does not contain DEHP even though the product...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: 84" (213 cm) 20 Drop Y-Type Blood Set w/200 Micron Filter Recalled by ICU...
The Issue: Some devices were labeled as Does not contain DEHP even though the product...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: 137" (348 cm) Y-Type Blood Set w/170 Micron Filter Recalled by ICU Medical,...
The Issue: Some devices were labeled as Does not contain DEHP even though the product...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: 175" (445 cm) Y-Type Blood Set w/170 Micron Blood Filter Recalled by ICU...
The Issue: Some devices were labeled as Does not contain DEHP even though the product...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: 125" (318 cm) Bifuse Blood Set w/170 Micron Filter Recalled by ICU Medical,...
The Issue: Some devices were labeled as Does not contain DEHP even though the product...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: 98" (249 cm) Y-Type Admin Set w/170 Micron Blood Filter Recalled by ICU...
The Issue: Some devices were labeled as Does not contain DEHP even though the product...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: 84" Y-Type Blood Set w/170 Micron Filter Recalled by ICU Medical, Inc. Due...
The Issue: Some devices were labeled as Does not contain DEHP even though the product...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: 128" (325 cm) Y-Type Blood Set with 170 Micron Filter Recalled by ICU...
The Issue: Some devices were labeled as Does not contain DEHP even though the product...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: 32" (81 cm) Appx 4.4 mL Recalled by ICU Medical, Inc. Due to Some devices...
The Issue: Some devices were labeled as Does not contain DEHP even though the product...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: 120" (305cm) Y-Type Blood Set w/170 Micron Filter Recalled by ICU Medical,...
The Issue: Some devices were labeled as Does not contain DEHP even though the product...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: 100" (254 cm) 20 Drop Y-Type Blood Set w/200 Micron Filter Recalled by ICU...
The Issue: Some devices were labeled as Does not contain DEHP even though the product...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: 119" Blood Set w/200 Micron Filter Recalled by ICU Medical, Inc. Due to Some...
The Issue: Some devices were labeled as Does not contain DEHP even though the product...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.