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. 2,411 recalls have been distributed to District of Columbia in the last 12 months.

47,654 total recalls
2,411 in last 12 months

Showing 3834138360 of 47,654 recalls

Medical DeviceDecember 15, 2014· Synthes, Inc.

Recalled Item: Malleable C- Retractor Recalled by Synthes, Inc. Due to Potential failure...

The Issue: Potential failure and/or corrosion of the internal spring of the retractor,...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 14, 2014· Villa Radiology Systems LLC

Recalled Item: Juno DFR X-ray system Recalled by Villa Radiology Systems LLC Due to The...

The Issue: The system does not provide the appropriate audible signal, permanent...

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

Class II — Potential Health HazardOngoing
DrugDecember 12, 2014· Anabolic Science Labs, LLC

Recalled Item: HALO-70 MEGA MASS BUILDER (4-chloro-17a-methyl-androst-1 Recalled by...

The Issue: Marketed without an approved NDA/ANDA - These products are being recalled...

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

Class I — Serious Health HazardOngoing
Refund
DrugDecember 12, 2014· Anabolic Science Labs, LLC

Recalled Item: SWOLL-250 SUPER MASS BUILDER QUAD STACK (18-Methylestr-4-en-3-one-17b-ol...

The Issue: Marketed without an approved NDA/ANDA - These products are being recalled...

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

Class I — Serious Health HazardOngoing
Refund
DrugDecember 12, 2014· Anabolic Science Labs, LLC

Recalled Item: M14-MENT ADVANCED MASS BUILDER (7a-Methyl-estra-4-en-3 Recalled by Anabolic...

The Issue: Marketed without an approved NDA/ANDA - These products are being recalled...

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

Class I — Serious Health HazardOngoing
Refund
DrugDecember 12, 2014· Anabolic Science Labs, LLC

Recalled Item: PROFESSIONAL FORMEXX BLACK (AromaMaXX 250mg: 13-dimethyl-1 Recalled by...

The Issue: Marketed without an approved NDA/ANDA - These products are being recalled...

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

Class I — Serious Health HazardOngoing
Refund
DrugDecember 12, 2014· Anabolic Science Labs, LLC

Recalled Item: 7-MENT ALPHA ADVANCED MASS BUILDER (7a-methyl-estra-4-en-3 Recalled by...

The Issue: Marketed without an approved NDA/ANDA - These products are being recalled...

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

Class I — Serious Health HazardOngoing
Refund
DrugDecember 12, 2014· Anabolic Science Labs, LLC

Recalled Item: M1-ALPHA LABS MEGA MASS BUILDER (M1A Recalled by Anabolic Science Labs, LLC...

The Issue: Marketed without an approved NDA/ANDA - These products are being recalled...

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

Class I — Serious Health HazardOngoing
Refund
DrugDecember 12, 2014· Anabolic Science Labs, LLC

Recalled Item: ESTRASTAIN PRO-ANABOLIC MASS AND HARDENING COMPLEX (Estra-4 Recalled by...

The Issue: Marketed without an approved NDA/ANDA - These products are being recalled...

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

Class I — Serious Health HazardOngoing
Refund
Medical DeviceDecember 12, 2014· Pointe Scientific, Inc.

Recalled Item: Pointe Scientific Creatinine Reagent Catalog number C7539-150 in vitro...

The Issue: Creatinine kit C7539-150 contains Creatinine reagent R1 that is labeled as...

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

Class III — Low RiskOngoing
Medical DeviceDecember 12, 2014· Teleflex, Inc.

Recalled Item: R¿SCH Curved Reinforced Endotracheal Tube: Rusch Reinforced Endotracheal...

The Issue: Teleflex Medical has issued an advisory notification for the RUSCH Curved...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 12, 2014· Biocare Medical Llc

Recalled Item: MUM-1 (Multiple myeloma oncogene-1) Recalled by Biocare Medical Llc Due to...

The Issue: Three lots of MUM-1 may not meet their labeled shelf life, as a drop in...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 11, 2014· Owen Mumford USA, Inc.

Recalled Item: Autopen Classic Automatic insulin delivery pen Recalled by Owen Mumford USA,...

The Issue: The dials in the Autopens are not working - the dial does not stay dialed,...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 11, 2014· Zimmer, Inc.

Recalled Item: Persona (TASP) Tibial Articular Surface Provisional Shim Recalled by Zimmer,...

The Issue: Potential for delay in surgery and/or ball bearings to be left in the wound....

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

Class II — Potential Health HazardOngoing
FoodDecember 10, 2014· Taylor Farms Pacific Inc. (MacArthur Facility)

Recalled Item: Citizen Chef Organic Superfood Salad- 4 Organic Salads. Power Greens...

The Issue: Undeclared Milk on individual units, outer packaging is labeled correctly.

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

Class II — Potential Health HazardOngoing
Refund
Medical DeviceDecember 10, 2014· Richard Wolf Medical Instruments Corp.

Recalled Item: The I-Cart is used to store Recalled by Richard Wolf Medical Instruments...

The Issue: The transformers installed on carts used for Richard Wolf medical video...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 10, 2014· Covidien

Recalled Item: Covidien Trellis-8 Peripheral Infusion System. Models CVT808015 Recalled by...

The Issue: A manufacturing error resulted in the risk of incorrect proximal and distal...

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

Class I — Serious Health HazardOngoing
Medical DeviceDecember 10, 2014· Covidien

Recalled Item: Covidien Trellis-6 Peripheral Infusion System. Models BVT608010V01 Recalled...

The Issue: A manufacturing error resulted in the risk of incorrect proximal and distal...

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

Class I — Serious Health HazardOngoing
DrugDecember 9, 2014· Akorn, Inc.

Recalled Item: Triamcinolone Acetonide Lotion USP Recalled by Akorn, Inc. Due to Failed...

The Issue: Failed Impurities/Degradation Specifications: The known impurity went out of...

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

Class III — Low RiskOngoing
Refund
DrugDecember 9, 2014· J. Strickland and Co

Recalled Item: sulfur8(R) medicated anti-dandruff conditioner Recalled by J. Strickland and...

The Issue: Failed pH specification: Product pH test value of 5.72 failed to meet its...

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

Class III — Low RiskOngoing
Refund