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. 2,423 recalls have been distributed to District of Columbia in the last 12 months.

47,654 total recalls
2,423 in last 12 months

Showing 3762137640 of 47,654 recalls

Medical DeviceFebruary 11, 2015· Intuitive Surgical, Inc.

Recalled Item: EndoWrist One Vessel Sealer Recalled by Intuitive Surgical, Inc. Due to...

The Issue: Intuitive Surgical has identified the potential for a certain, small portion...

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 11, 2015· EXP Pharmaceutical Services Corp

Recalled Item: Medical Device Exchange Round Diamond Bur Extra Coarse Recalled by EXP...

The Issue: EXP did not register as a medical device establishment, list the devices...

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 11, 2015· EXP Pharmaceutical Services Corp

Recalled Item: Medical Device Exchange Wire (sternotomy wire) Recalled by EXP...

The Issue: EXP did not register as a medical device establishment, list the devices...

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 11, 2015· EXP Pharmaceutical Services Corp

Recalled Item: Medical Device Exchange SECURESTRAP 5mm Absorbable Strap Fixation Device...

The Issue: EXP did not register as a medical device establishment, list the devices...

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 11, 2015· EXP Pharmaceutical Services Corp

Recalled Item: Medical Device Exchange ETS FLEX 45 ENDOSCOPIC ARTICULATING LINEAR CUTTER...

The Issue: EXP did not register as a medical device establishment, list the devices...

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 11, 2015· Intuitive Surgical, Inc.

Recalled Item: EndoWrist One Vessel Sealer Recalled by Intuitive Surgical, Inc. Due to...

The Issue: Intuitive Surgical has identified the potential for a certain, small portion...

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 11, 2015· EXP Pharmaceutical Services Corp

Recalled Item: Medical Device Exchange -Suction Coagulator Recalled by EXP Pharmaceutical...

The Issue: EXP did not register as a medical device establishment, list the devices...

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 11, 2015· Sybron Dental Specialties

Recalled Item: Outer cardboard box labeling: Pinnacle Cure Sleeve Recalled by Sybron Dental...

The Issue: Cases of Cure Sleeve labeled with part number 4513, which fits 13mm tips,...

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 11, 2015· EXP Pharmaceutical Services Corp

Recalled Item: Medical Device Exchange 2.15MMX22MM Fluted Spiral Router for CRANI-A...

The Issue: EXP did not register as a medical device establishment, list the devices...

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 11, 2015· EXP Pharmaceutical Services Corp

Recalled Item: Medical Device Exchange PT WIRE 300 Recalled by EXP Pharmaceutical Services...

The Issue: EXP did not register as a medical device establishment, list the devices...

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 11, 2015· EXP Pharmaceutical Services Corp

Recalled Item: Medical Device Exchange - Silicone Round Drain Recalled by EXP...

The Issue: EXP did not register as a medical device establishment, list the devices...

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 11, 2015· EXP Pharmaceutical Services Corp

Recalled Item: Medical Device Exchange - Auto Suture Endo Universal 65¿¿ 4mm Recalled by...

The Issue: EXP did not register as a medical device establishment, list the devices...

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 11, 2015· EXP Pharmaceutical Services Corp

Recalled Item: Medical Device Exchange Angio-Seal VIP Platform/Vascular Closure Device 6F...

The Issue: EXP did not register as a medical device establishment, list the devices...

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 11, 2015· EXP Pharmaceutical Services Corp

Recalled Item: Medical Device Exchange Round Fluted Bur Soft Touch Recalled by EXP...

The Issue: EXP did not register as a medical device establishment, list the devices...

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 11, 2015· EXP Pharmaceutical Services Corp

Recalled Item: Medical Device Exchange - Dilating Tip Trocar w/Stability Sleeve 12mm...

The Issue: EXP did not register as a medical device establishment, list the devices...

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 11, 2015· EXP Pharmaceutical Services Corp

Recalled Item: Medical Device Exchange Round Fluted Bur Aggressive Recalled by EXP...

The Issue: EXP did not register as a medical device establishment, list the devices...

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 11, 2015· EXP Pharmaceutical Services Corp

Recalled Item: Medical Device Exchange -SYSTEM Recalled by EXP Pharmaceutical Services Corp...

The Issue: EXP did not register as a medical device establishment, list the devices...

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 11, 2015· EXP Pharmaceutical Services Corp

Recalled Item: Medical Device Exchange 10MM VASCULAR Recalled by EXP Pharmaceutical...

The Issue: EXP did not register as a medical device establishment, list the devices...

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

Class II — Potential Health HazardOngoing
FoodFebruary 11, 2015· Sunfood Corportation

Recalled Item: Organic Sacha Inchi Powder Recalled by Sunfood Corportation Due to Sunfood...

The Issue: Sunfood is recalling Sacha Inchi Powder because it has the potential to be...

Recommended Action: Do not consume. Return to store for a refund or discard.

Class II — Potential Health HazardOngoing
Refund
Medical DeviceFebruary 10, 2015· Tosoh Bioscience, Inc.

Recalled Item: G7 Variant Elution Buffer HiS no. 1 (M) component of Recalled by Tosoh...

The Issue: The G7 Variant Elution Buffer HiS no. 1 (M) is incorrectly labeled with an...

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

Class III — Low RiskOngoing