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. 2,591 recalls have been distributed to District of Columbia in the last 12 months.

47,654 total recalls
2,591 in last 12 months

Showing 1118111200 of 27,451 recalls

Medical DeviceJuly 15, 2020· Hager & Meisinger Gmbh

Recalled Item: SINGLES Carbide US-No. FG556 Recalled by Hager & Meisinger Gmbh Due to...

The Issue: US-dates between the product package label and the bar code display.

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 14, 2020· Thomas Scientific

Recalled Item: Wuxi Nest Recalled by Thomas Scientific Due to The firm is replacing all...

The Issue: The firm is replacing all tubes that were manufactured and distributed prior...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 14, 2020· Siemens Medical Solutions USA, Inc

Recalled Item: Cios Alpha (VA20) - Model: 10308191 Cios Alpha (VA30) - Recalled by Siemens...

The Issue: Hardware error- Hot Plugging feature could cause an electrical malfunction...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 13, 2020· OraSure Technologies, Inc.

Recalled Item: Orasure Technologies Interept Benzodiazopene Miro-Plate EIA-Benzo EIA 2...

The Issue: Incorrect lot number for Standard Oral Fluid Negative Calibrator on...

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

Class III — Low RiskOngoing
Medical DeviceJuly 13, 2020· Ortho-Clinical Diagnostics

Recalled Item: VITROS Chemistry Products TBIL Slides- 5 PACK/300 SLDS In vitro Recalled by...

The Issue: Etrombopag Interference for VITROS Chemistry Products: TBIL Slides, VITROS...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 13, 2020· Ortho-Clinical Diagnostics

Recalled Item: VITROS XT Chemistry Products TBIL-ALKP Slides (ALKP is not affected)...

The Issue: Etrombopag Interference for VITROS Chemistry Products: TBIL Slides, VITROS...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 13, 2020· Ortho-Clinical Diagnostics

Recalled Item: VITROS Chemistry Products BuBc Slides - in vitro diagnostic use Recalled by...

The Issue: Etrombopag Interference for VITROS Chemistry Products: TBIL Slides, VITROS...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 13, 2020· OraSure Technologies, Inc.

Recalled Item: Orasure Technologies Interept Benzodiazopene Miro-Plate EIA-Benzo EIA 5plate...

The Issue: Incorrect lot number for Standard Oral Fluid Negative Calibrator on...

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

Class III — Low RiskOngoing
Medical DeviceJuly 13, 2020· Aesculap Implant Systems LLC

Recalled Item: ENNOVATE MIS REMOVALKEY SHORT Recalled by Aesculap Implant Systems LLC Due...

The Issue: Fracture or breakage of the spinal fixation arm at the downtube instrument...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 9, 2020· Medline Industries Inc

Recalled Item: Endoscopic Cleaning Brush - Product Usage: Endoscopic cleaning brushes are...

The Issue: Potential risk of brush detachment during cleaning.

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 8, 2020· Flower Orthopedics Corporation

Recalled Item: Calcaneus Plate Recalled by Flower Orthopedics Corporation Due to The...

The Issue: The contract manufacturer of the calcaneus plate inadvertently used the...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 8, 2020· Flower Orthopedics Corporation

Recalled Item: Calcaneus Plate Recalled by Flower Orthopedics Corporation Due to The...

The Issue: The contract manufacturer of the calcaneus plate inadvertently used the...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 8, 2020· Flower Orthopedics Corporation

Recalled Item: Calcaneus Plate Recalled by Flower Orthopedics Corporation Due to The...

The Issue: The contract manufacturer of the calcaneus plate inadvertently used the...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 8, 2020· Flower Orthopedics Corporation

Recalled Item: Calcaneus Plate Recalled by Flower Orthopedics Corporation Due to The...

The Issue: The contract manufacturer of the calcaneus plate inadvertently used the...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 8, 2020· Flower Orthopedics Corporation

Recalled Item: Calcaneus Plate Recalled by Flower Orthopedics Corporation Due to The...

The Issue: The contract manufacturer of the calcaneus plate inadvertently used the...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 8, 2020· Flower Orthopedics Corporation

Recalled Item: Calcaneus Plate Recalled by Flower Orthopedics Corporation Due to The...

The Issue: The contract manufacturer of the calcaneus plate inadvertently used the...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 8, 2020· New Wave Endo-Surgical, Corp.

Recalled Item: M-Close Kit Recalled by New Wave Endo-Surgical, Corp. Due to The plastic...

The Issue: The plastic housing on the device may fracture

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 6, 2020· ICU Medical, Inc.

Recalled Item: 126" (320 cm) 16.4 ml Recalled by ICU Medical, Inc. Due to Identification of...

The Issue: Identification of a potential manufacturing defect on the internal surface...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 6, 2020· ICU Medical, Inc.

Recalled Item: 2 Gang 4-Way NanoClave Stopcock Manifold w/Rotating Luer Recalled by ICU...

The Issue: Identification of a potential manufacturing defect on the internal surface...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 6, 2020· ICU Medical, Inc.

Recalled Item: 9.5 IN (24cm)APPX 1.1ml SMALLBORE TRIFUSE SET Recalled by ICU Medical, Inc....

The Issue: Identification of a potential manufacturing defect on the internal surface...

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

Class II — Potential Health HazardOngoing