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. 1,033 recalls have been distributed to District of Columbia in the last 12 months.
Showing 11781–11800 of 47,654 recalls
Recalled Item: Hill-Rom PRO+ MRS Surface For Versacare With X-Ray mattress Recalled by...
The Issue: The failure mode on the affected mattresses can cause a reduction in the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Hill-Rom PRO+ 36" MRS Surface mattress Recalled by Baxter Healthcare...
The Issue: The failure mode on the affected mattresses can cause a reduction in the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: UroLift System Recalled by Neotract Inc Due to There is the potential that...
The Issue: There is the potential that during implant deployment, the device may not...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Stryker 2.3mm Tapered Router Recalled by Stryker Instruments Due to There is...
The Issue: There is a potential for the core diameter to be undersized, which may lead...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Hill-Rom Centrella Pro+ 40" Surface mattress Recalled by Baxter Healthcare...
The Issue: The failure mode on the affected mattresses can cause a reduction in the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ZEISS Axio Observer 5 microscope Recalled by Zeiss, Carl Inc Due to An...
The Issue: An incorrect Unique Device Identification (UDI) label was installed on some...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: SIGNA Premier magnetic resonance scanner Recalled by GE Healthcare, LLC Due...
The Issue: Under rare conditions, SIGNA Premier gradient coils could result in elevated...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Hill-Rom Centrella Pro+ 36" Surface mattress Recalled by Baxter Healthcare...
The Issue: The failure mode on the affected mattresses can cause a reduction in the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Hill-Rom Centrella Pro+ 36" Surface With X-Ray mattress Recalled by Baxter...
The Issue: The failure mode on the affected mattresses can cause a reduction in the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Medline Sprinter OTW Recalled by Medtronic Inc Due to Luer has balloon...
The Issue: Luer has balloon diameter printed as "2.25mmx12mm" instead of the correct...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Hydrogen Peroxide Topical Solution Recalled by Vi-Jon, LLC Due to Labeling:...
The Issue: Labeling: Label Mix-Up-The primary label on the front of the bottles have...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Daytrana (methylphenidate transdermal system) Delivers 10 mg over 9 hours...
The Issue: Defective Delivery System: Customer complaints received for ripping patches...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: ST IVES BLKHD CLRNG GREEN TEA SCRUB 6 OZ SKU Recalled by Family Dollar...
The Issue: CGMP Deviations: product held outside appropriate storage temperature...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: QP COUGH COLD TABLET 16 CT distributed to specific Family Recalled by Family...
The Issue: CGMP Deviations: product held outside appropriate storage temperature...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: NPX ENEMA 4.5 FL OZ 2 PK distributed to specific Recalled by Family Dollar...
The Issue: CGMP Deviations: product held outside appropriate storage temperature...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: MIDOL COMPLETE CAPLET 16 CT SKU 913028 QP MENSTRUAL RELIEF Recalled by...
The Issue: CGMP Deviations: product held outside appropriate storage temperature...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: GS ANTI DIARRHEAL LOPERAMIDE CAPLET 12 CT SKU 915632 IMODIUM Recalled by...
The Issue: CGMP Deviations: product held outside appropriate storage temperature...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: QP SUDFEDRINE PE MAX STRENGTH TBLT 24 CT distributed to Recalled by Family...
The Issue: CGMP Deviations: product held outside appropriate storage temperature...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: QP COLD MULTI SYMPTM DAY NITE CPLT 24 CT distributed Recalled by Family...
The Issue: CGMP Deviations: product held outside appropriate storage temperature...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: GOOD SENSE SORE THROAT SPRAY CHERRY 6 FL OZ distributed Recalled by Family...
The Issue: CGMP Deviations: product held outside appropriate storage temperature...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.