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. 2,485 recalls have been distributed to District of Columbia in the last 12 months.

47,654 total recalls
2,485 in last 12 months

Showing 2246122480 of 47,654 recalls

Medical DeviceMarch 14, 2019· Nobel Biocare Usa Llc

Recalled Item: Implant Retrieval Instrument CC RP & Tri Ch Hex WP Recalled by Nobel Biocare...

The Issue: Due to a problem in the packaging sealing process at the supplier of the...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceMarch 14, 2019· Nobel Biocare Usa Llc

Recalled Item: Implant Retrieval Instrument CC 3.0 31 mm- Product Usage: They Recalled by...

The Issue: Due to a problem in the packaging sealing process at the supplier of the...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceMarch 14, 2019· Nobel Biocare Usa Llc

Recalled Item: Implant Retrieval Instrument CC NP & Ext Hex WP 22 Recalled by Nobel Biocare...

The Issue: Due to a problem in the packaging sealing process at the supplier of the...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceMarch 14, 2019· Nobel Biocare Usa Llc

Recalled Item: Dense Bone Drill NP 3.5x16 mm Single-Pat - Product Usage: Recalled by Nobel...

The Issue: Due to a problem in the packaging sealing process at the supplier of the...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceMarch 13, 2019· Medical Components, Inc dba MedComp

Recalled Item: 14F x 30CM SLX Double Lumen Full Tray Hemodialysis catheter insertion kits...

The Issue: Tray label indicates the kits are packaged with a 15F "valved" peelable...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceMarch 13, 2019· Vyaire Medical

Recalled Item: enFlow Disposable Cartridge with IV Extension Set Recalled by Vyaire Medical...

The Issue: Testing has demonstrated aluminum elution from the enFlow Disposable...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class I — Serious Health HazardOngoing
Medical DeviceMarch 13, 2019· Exactech, Inc.

Recalled Item: Truliant Tibial Fit Tray Cemented SZ 3F / 3T Recalled by Exactech, Inc. Due...

The Issue: 2.5 Truliant Fit Trays were mismarked as 3

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceMarch 13, 2019· COVIDIEN LLC

Recalled Item: Procedure kits include devices from the affected lots distributed OUS...

The Issue: Sterilization method used was not consistent with the labeling and the...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceMarch 13, 2019· Medical Components, Inc dba MedComp

Recalled Item: 14F x 24CM SLX Double Lumen Full Tray Hemodialysis catheter insertion kits...

The Issue: Tray label indicates the kits are packaged with a 15F "valved" peelable...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceMarch 13, 2019· Medical Components, Inc dba MedComp

Recalled Item: 14F x 20CM SLX Double Lumen Full Tray Hemodialysis catheter insertion kits...

The Issue: Tray label indicates the kits are packaged with a 15F "valved" peelable...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceMarch 13, 2019· COVIDIEN LLC

Recalled Item: Covidien Endo Clinch II Auto Suture Grasper Recalled by COVIDIEN LLC Due to...

The Issue: Sterilization method used was not consistent with the labeling and the...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceMarch 13, 2019· COVIDIEN LLC

Recalled Item: Covidien Endo Grasp Auto Suture Grasper 5mm The Recalled by COVIDIEN LLC Due...

The Issue: Sterilization method used was not consistent with the labeling and the...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceMarch 13, 2019· Vyaire Medical

Recalled Item: enFlow Disposable Cartridge Recalled by Vyaire Medical Due to Testing has...

The Issue: Testing has demonstrated aluminum elution from the enFlow Disposable...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class I — Serious Health HazardOngoing
DrugMarch 13, 2019· Advanced Pharma Inc.

Recalled Item: Heparin 10 Units/10 mL 10 Units in 0.45% Sodium Chloride Recalled by...

The Issue: Lack of Assurance of Sterility

Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.

Class II — Potential Health HazardOngoing
Refund
DrugMarch 13, 2019· Advanced Pharma Inc.

Recalled Item: HYDROmorphone HCl 1 mg in 0.9% Sodium Chloride Recalled by Advanced Pharma...

The Issue: Lack of Assurance of Sterility

Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.

Class II — Potential Health HazardOngoing
Refund
DrugMarch 13, 2019· Advanced Pharma Inc.

Recalled Item: Morphine Sulfate 30 mg/30 mL (1 mg/mL) Injectable Solution Morphine Recalled...

The Issue: Lack of Assurance of Sterility

Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.

Class II — Potential Health HazardOngoing
Refund
DrugMarch 13, 2019· Advanced Pharma Inc.

Recalled Item: fentaNYL 1000 mcg/100 mL Injectable Solution Fentanyl 0.9% Sodium Chloride...

The Issue: Lack of Assurance of Sterility

Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.

Class II — Potential Health HazardOngoing
Refund
DrugMarch 13, 2019· Advanced Pharma Inc.

Recalled Item: Phenylephrine HCl Recalled by Advanced Pharma Inc. Due to Lack of Assurance...

The Issue: Lack of Assurance of Sterility

Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.

Class II — Potential Health HazardOngoing
Refund
DrugMarch 13, 2019· Advanced Pharma Inc.

Recalled Item: Phenylephrine HCl Recalled by Advanced Pharma Inc. Due to Lack of Assurance...

The Issue: Lack of Assurance of Sterility

Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.

Class II — Potential Health HazardOngoing
Refund
DrugMarch 13, 2019· Advanced Pharma Inc.

Recalled Item: 2% Lidocaine HCl Injectable Solution Recalled by Advanced Pharma Inc. Due to...

The Issue: Lack of Assurance of Sterility

Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.

Class II — Potential Health HazardOngoing
Refund