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. 2,459 recalls have been distributed to District of Columbia in the last 12 months.

47,654 total recalls
2,459 in last 12 months

Showing 2626126280 of 47,654 recalls

Medical DeviceDecember 27, 2017· Mako Surgical Corporation

Recalled Item: Makoplasty RIO Standard System Recalled by Mako Surgical Corporation Due to...

The Issue: Communication-connection error.

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 22, 2017· DePuy Mitek, Inc., a Johnson & Johnson Co.

Recalled Item: LATARJET EXPERIENCE Sharp Curved Ostetome Product Usage: The Latarjet...

The Issue: Reports of product loosening or coming unscrewed from the handle.

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

Class II — Potential Health HazardOngoing
DrugDecember 22, 2017· Hetero Labs Limited Unit V

Recalled Item: Famciclovir Tablets Recalled by Hetero Labs Limited Unit V Due to...

The Issue: Temperature Abuse: Complaints of tablets being wet and stuck together with...

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

Class II — Potential Health HazardOngoing
Refund
DrugDecember 22, 2017· Hetero Labs, Ltd. - Unit III

Recalled Item: Simvastatin Tablets Recalled by Hetero Labs, Ltd. - Unit III Due to Presence...

The Issue: Presence of foreign substance: metallic razor blade was found in one bottle.

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

Class III — Low RiskOngoing
Refund
FoodDecember 22, 2017· Harris Teeter Distribution Ctr

Recalled Item: Harris Teeter's HT Traders Mama Biscotti Mini Biscotti Recalled by Harris...

The Issue: Undeclared allergen: Almonds

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

Class II — Potential Health HazardOngoing
Refund
FoodDecember 22, 2017· Nodine's Smokehouse Inc.

Recalled Item: Smoked salmon in 1.5 oz. and 8 oz. packages Recalled by Nodine's Smokehouse...

The Issue: Product may be contaminated with Listeria monocytogenes.

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

Class I — Serious Health HazardOngoing
Refund
FoodDecember 22, 2017· Coconuthead, LLC

Recalled Item: CO YO Coconut Yogurt Alternative CHOCOLATE Recalled by Coconuthead, LLC Due...

The Issue: Coconuthead LLC is recalling CO YO Coconut Yogurt Alternative CHOCOLATE due...

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

Class II — Potential Health HazardOngoing
Refund
FoodDecember 21, 2017· Nutricia North America

Recalled Item: SHS Wel-Plan Wheat and Corn Strach Baking Mix Recalled by Nutricia North...

The Issue: Nutricia North America, Inc. has decided to recall SHS Wel-Plan Baking Mix ,...

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

Class II — Potential Health HazardOngoing
Refund
DrugDecember 21, 2017· Taro Pharmaceuticals U.S.A., Inc.

Recalled Item: Clobetasol Propionate Cream USP Recalled by Taro Pharmaceuticals U.S.A.,...

The Issue: Failed Content Uniformity Specifications

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

Class III — Low RiskOngoing
Refund
Medical DeviceDecember 21, 2017· W & H DentalWerk Burmoos GMBH - Site 1

Recalled Item: Foot Controls Model: S-N1 and S-N2 Product Usage: Variable foot Recalled by...

The Issue: During continuous postmarket surveillance activities, we have noticed a...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 21, 2017· DePuy Orthopaedics, Inc.

Recalled Item: (1) Sigma HP Cemented Trochlea Size 1 Narrow Left Recalled by DePuy...

The Issue: The SIGMA¿ HP PFJ Cemented Trochlear Implants, a standalone component of the...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 20, 2017· Zimmer Biomet, Inc.

Recalled Item: ACE Trochanteric Nail System ATN AR SCREW 60MM STERILE ATN Recalled by...

The Issue: Zimmer Biomet is conducting a medical device recall for the ACE Trochanteric...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 20, 2017· Zimmer Biomet, Inc.

Recalled Item: ACE Trochanteric Nail System STER TROC NAIL 125 DEG X Recalled by Zimmer...

The Issue: Zimmer Biomet is conducting a medical device recall for the ACE Trochanteric...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 20, 2017· Philips Electronics North America Corporation

Recalled Item: Allura Xper FD and and Xper FD ORT - Philips Recalled by Philips Electronics...

The Issue: Extra monitors, so called 7th or 8th monitor, mounted on the Monitor Ceiling...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 20, 2017· Boston Scientific Corporation

Recalled Item: SpyScope DS Access and Delivery diagnostic biliary catheter Recalled by...

The Issue: Certain lots of devices may have the working channel sleeve protruding from...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 20, 2017· Zimmer Biomet, Inc.

Recalled Item: ACE Trochanteric Nail System STER L H TROC NAIL 320X9X125 Recalled by Zimmer...

The Issue: Zimmer Biomet is conducting a medical device recall for the ACE Trochanteric...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 20, 2017· Zimmer Biomet, Inc.

Recalled Item: ACE Trochanteric Nail System STER TROC LAG SCR 70 MM Recalled by Zimmer...

The Issue: Zimmer Biomet is conducting a medical device recall for the ACE Trochanteric...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 20, 2017· Zimmer Biomet, Inc.

Recalled Item: ACE Trochanteric Nail System ACE TROCH NAIL 125 DEG. X Recalled by Zimmer...

The Issue: Zimmer Biomet is conducting a medical device recall for the ACE Trochanteric...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 20, 2017· Zimmer Biomet, Inc.

Recalled Item: ACE Trochanteric Nail System STER TROC END CAP STER TROC Recalled by Zimmer...

The Issue: Zimmer Biomet is conducting a medical device recall for the ACE Trochanteric...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 20, 2017· Zimmer Biomet, Inc.

Recalled Item: ACE Trochanteric Nail System STER TROC NAIL 180X13X140 STER TROC Recalled by...

The Issue: Zimmer Biomet is conducting a medical device recall for the ACE Trochanteric...

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

Class II — Potential Health HazardOngoing