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. 2,360 recalls have been distributed to District of Columbia in the last 12 months.
Showing 47241–47260 of 47,654 recalls
Recalled Item: Poly stat Flu A & B Test Manufactured for Polymedco Recalled by Princeton...
The Issue: There have been reports of dual positive (Flu A + Flu B positive) results...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Status Flu A + B Test Manufactured by Princeton Bio Recalled by Princeton...
The Issue: There have been reports of dual positive (Flu A + Flu B positive) results...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Orasure QuickFlu Rapid A+B Test Manufactured for OraSure Technologies...
The Issue: There have been reports of dual positive (Flu A + Flu B positive) results...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: BLOM-SINGER indwelling TEP Occluder Recalled by Helix Medical LLC Due to...
The Issue: Helix Medical LLC is recalling the BLOM-SINGER indwelling TEP Occluder due...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Pinnacle Hip Solutions ALTRX Polyethylene Acetabular Liner Recalled by DePuy...
The Issue: DePuy Orthopaedics, Inc. (DePuy) is issuing a voluntary recall of one lot of...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: i-STAT cTnI cartridges Product Usage: The i-STAT cTnl test is Recalled by...
The Issue: Abbott Point of Care has determined that i-Stat CTNL cartridges have the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: S4 Cervical (S4C) Revision Instruments (FW099R and FW101R). The S4C Recalled...
The Issue: Aesculap Implant Systems, LLC has initiated a voluntary removal of the S4...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: GE Healthcare Quasar Nuclear Medicine System Recalled by GE Healthcare, LLC...
The Issue: Accelerated fatigue of the lateral axis motion subsystem of the Infinia...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: BD Vacutainer PST Gel and Lithium Heparin (LH) Recalled by Becton Dickinson...
The Issue: BD is conducting a recall of the BD Vacutainer Plus Plastic Plasma Separator...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: I-STAT PT/INR cartridge Abbott Point of Care Inc. Abbott Park Recalled by...
The Issue: The i-STAT PT/INR cartridges have the potential to exhibit incorrectly...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Thyro-Tab.075 mg. Recalled by Lloyd Inc Due to Subpotent (Single Ingredient...
The Issue: Subpotent (Single Ingredient Drug): Low assay at the 6-month test interval.
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Levothroid (levothyroxine sodium tablets Recalled by Lloyd Inc Due to...
The Issue: Subpotent (Single Ingredient Drug): Low assay at the 6-month test interval.
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Lithium Thionyl non-rechargeable disposable battery pack P/N 350-0294-01...
The Issue: Braemar has recently became aware of a battery related incident that...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Siemens syngo.plaza. Radiological image processing system Recalled by...
The Issue: Siemens became aware of a potential malfunction when using syngo.plaza with...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Man King Capsules Recalled by www.vitaminbestbuy.com Due to Marketed Without...
The Issue: Marketed Without an Approved ANDA/NDA: presence of sildenafil.
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Japan Weight Loss Blue Capsules Recalled by www.vitaminbestbuy.com Due to...
The Issue: Marketed Without an Approved ANDA/NDA: presence of sibutramine
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Hard Ten Days Capsule Recalled by www.vitaminbestbuy.com Due to Marketed...
The Issue: Marketed Without an Approved ANDA/NDA: presence of sildenafil
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Thyroglobulin Antibody (TgAB) Calibrator - Product Usage: intended for IN...
The Issue: Some combinations of Calibrator lots and AlA PACKS resulted in Calibrator #6...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: TX1 Tissue Removal System Console. Model: TX1 TX1 Tissue Removal Recalled by...
The Issue: Two reasons for recall. 1. Incorrect pressure relief valve installed inside...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: The brand name of the device is AlgiNot Recalled by Kerr Corporation Due to...
The Issue: The firm recalled the product because it may cure harder than expected...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.