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. 2,448 recalls have been distributed to District of Columbia in the last 12 months.

47,654 total recalls
2,448 in last 12 months

Showing 2566125680 of 27,451 recalls

Medical DeviceFebruary 26, 2013· Cooper Surgical, Inc.

Recalled Item: Cooper Surgical Incontinence Dish w/ Support Pessary #0 Recalled by Cooper...

The Issue: Pessary mislabeled outer package may not the size of the product contained...

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

Class III — Low RiskOngoing
Medical DeviceFebruary 26, 2013· Cooper Surgical, Inc.

Recalled Item: LEEP REDIKIT Product No. 6060 In a Loop Electrosurgical Excision Recalled by...

The Issue: LEEP RediKit Products (for use in Loop Electrosurgical Excision Procedures)...

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 26, 2013· Hill-Rom, Inc.

Recalled Item: TotalCare SpO2RT2 bed. Product Usage: Bed Recalled by Hill-Rom, Inc. Due to...

The Issue: In certain situations a software problem with the TotalCare SpO2RT¿ 2 bed...

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 26, 2013· Cooper Surgical, Inc.

Recalled Item: Cooper Surgical Gellhorn Flexible Pessary 3" Recalled by Cooper Surgical,...

The Issue: Pessary mislabeled outer package may not the size of the product contained...

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

Class III — Low RiskOngoing
Medical DeviceFebruary 26, 2013· Cooper Surgical, Inc.

Recalled Item: Cooper Surgical Incontinence Ring Flexible Pessary #4 Recalled by Cooper...

The Issue: Pessary mislabeled outer package may not the size of the product contained...

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

Class III — Low RiskOngoing
Medical DeviceFebruary 26, 2013· Cooper Surgical, Inc.

Recalled Item: Cooper Surgical Gellhorn Flexible Pessary -2 3/4" Recalled by Cooper...

The Issue: Pessary mislabeled outer package may not the size of the product contained...

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

Class III — Low RiskOngoing
Medical DeviceFebruary 26, 2013· Cooper Surgical, Inc.

Recalled Item: Cooper Surgical Incontinence Dish Folding Pessary #0 Recalled by Cooper...

The Issue: Pessary mislabeled outer package may not the size of the product contained...

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

Class III — Low RiskOngoing
Medical DeviceFebruary 26, 2013· Cooper Surgical, Inc.

Recalled Item: Cooper Surgical Cube Pessary 1 5/8"" Recalled by Cooper Surgical, Inc. Due...

The Issue: Pessary mislabeled outer package may not the size of the product contained...

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

Class III — Low RiskOngoing
Medical DeviceFebruary 26, 2013· Cooper Surgical, Inc.

Recalled Item: Cooper Surgical Incontinence Dish Folding Pessary #0 Recalled by Cooper...

The Issue: Pessary mislabeled outer package may not the size of the product contained...

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

Class III — Low RiskOngoing
Medical DeviceFebruary 26, 2013· Intio Inc

Recalled Item: INTIO Inc. Recalled by Intio Inc Due to INTIO Inc. distributed a SVM User's...

The Issue: INTIO Inc. distributed a SVM User's Manual and it has an editing mistake...

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 26, 2013· Cooper Surgical, Inc.

Recalled Item: Cooper Surgical Cube Pessary w/Drainage Holes #0"1" Recalled by Cooper...

The Issue: Pessary mislabeled outer package may not the size of the product contained...

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

Class III — Low RiskOngoing
Medical DeviceFebruary 26, 2013· Neurotherm, Inc.

Recalled Item: Neurotherm Curved Radiofrequency (RF) cannnula 10 cm 18 gauge Recalled by...

The Issue: Straight needle labeled as a curved needle

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 25, 2013· Baxter Healthcare Corp.

Recalled Item: MiniCap Extended Life PD Transfer Set (6") with Twist Clamp. Recalled by...

The Issue: Labeling Revision: Additional instructions for the use of peritoneal...

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 25, 2013· Baxter Healthcare Corp.

Recalled Item: MiniCap Extended Life PD Transfer Set Extra Short (4") with Recalled by...

The Issue: Labeling Revision: Additional instructions for the use of peritoneal...

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 25, 2013· Baxter Healthcare Corp.

Recalled Item: CAPD Solution Transfer Set with Locking Connector. Product Code: 5C4160....

The Issue: Labeling Revision: Additional instructions for the use of peritoneal...

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 25, 2013· Baxter Healthcare Corp.

Recalled Item: MiniCap Extended Life PD Transfer Set. Product Code 5C4449. intended...

The Issue: Labeling Revision: Additional instructions for the use of peritoneal...

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 25, 2013· Nova Biomedical Corporation

Recalled Item: Nova StatStrip Xpress Glu-Test Strips (Glucose test strips) Catalog # 42214...

The Issue: Glucose test strips reports no result message when tested

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 25, 2013· Nipro Diagnostics, Inc.

Recalled Item: Duane Reade TRUEtrack monitor kit Recalled by Nipro Diagnostics, Inc. Due to...

The Issue: Meter kit outer boxes containing 10 ct. test strips state incorrect storage...

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 25, 2013· Symbios Medical Products, LLC

Recalled Item: GOPump Elastometric infusion PumpKit with/ and without accesssories all...

The Issue: Received 2 complaints out of 458 distributed pumps in this lot, where flow...

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

Class I — Serious Health HazardOngoing
Medical DeviceFebruary 25, 2013· Lifescan Inc

Recalled Item: LifeScan brand OneTouch¿ Ultra Control Solution Recalled by Lifescan Inc Due...

The Issue: When OneTouch¿ Ultra and OneTouch¿ Select test strips are tested with Ultra...

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

Class II — Potential Health HazardOngoing