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 26101–26120 of 27,451 recalls
Recalled Item: Biosense Webster MobiCath Bi-Directional Guiding Sheath. Small Curve catalog...
The Issue: Greatbatch Medical observed some anomalies of the inner lumen of the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Stryker Orthobiologics Aliquot Delivery System Manual Surgical Instrument -...
The Issue: There have been a few reported cases of the catheter breaking when removing...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Stryker Orthobiologics Aliquot Delivery System Manual Surgical Instrument -...
The Issue: There have been a few reported cases of the catheter breaking when removing...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Stryker Orthobiologics Aliquot Delivery System Manual Surgical Instrument -...
The Issue: There have been a few reported cases of the catheter breaking when removing...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Stryker Orthobiologics Aliquot Delivery System Manual Surgical Instrument -...
The Issue: There have been a few reported cases of the catheter breaking when removing...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Stryker Orthobiologics Aliquot Delivery System Manual Surgical Instrument -...
The Issue: There have been a few reported cases of the catheter breaking when removing...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Stryker Orthobiologics Aliquot Delivery System Manual Surgical Instrument -...
The Issue: There have been a few reported cases of the catheter breaking when removing...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Stryker Orthobiologics Aliquot Delivery System Manual Surgical Instrument -...
The Issue: There have been a few reported cases of the catheter breaking when removing...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Stryker Orthobiologics Aliquot Delivery System Manual Surgical Instrument -...
The Issue: There have been a few reported cases of the catheter breaking when removing...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Stryker Orthobiologics Aliquot Delivery System Manual Surgical Instrument -...
The Issue: There have been a few reported cases of the catheter breaking when removing...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Stryker Orthobiologics Aliquot Delivery System Manual Surgical Instrument -...
The Issue: There have been a few reported cases of the catheter breaking when removing...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Stryker Orthobiologics Aliquot Delivery System Manual Surgical Instrument -...
The Issue: There have been a few reported cases of the catheter breaking when removing...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Stryker Orthobiologics Aliquot Delivery System Manual Surgical Instrument -...
The Issue: There have been a few reported cases of the catheter breaking when removing...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Stryker Orthobiologics Aliquot Delivery System Manual Surgical Instrument -...
The Issue: There have been a few reported cases of the catheter breaking when removing...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: GE Healthcare Recalled by GE Healthcare, LLC Due to GE Healthcare became...
The Issue: GE Healthcare became aware of a potential issue associated with the LOGIQ e...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: SynchroMed EL Recalled by Medtronic Neuromodulation Due to Medtronic...
The Issue: Medtronic notified Healthcare Professionals of the impact of unapproved...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Philips IntelliVue Information Center/Client and Philips IntelliVue...
The Issue: Internal audio cable may have diminished retention force due to damaged...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: AVAIRA (enfilcon A) Soft (Hydrophilic) Daily Wear Toric Contact Lenses...
The Issue: The lenses exceeded the acceptance limit for silicone oil residual.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Medtronic SynchroMed II Recalled by Medtronic Neuromodulation Due to...
The Issue: Medtronic notified Healthcare Professionals of the impact of unapproved...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: EnteraLite Infinity Enteral Feeding Pump identified with the following list...
The Issue: MOOG Medical Devices Group is conducting a voluntary for a limited set of...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.