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 3744137460 of 47,654 recalls

Medical DeviceMarch 9, 2015· Fujifilm Medical Systems U.S.A., Inc.

Recalled Item: Fujifilm Endoscope Model ED-530XT Product Usage: This product is a Recalled...

The Issue: Fujifilm is reporting a corrective action due to an FDA inspection.

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

Class II — Potential Health HazardOngoing
FoodMarch 9, 2015· Cuisine Innovations LLC dba Bon Appetizers, LLC

Recalled Item: Black Bean Burger 4.5 oz 40 pieces Net Wt. 11.25 Recalled by Cuisine...

The Issue: Products may contain cumin which may contain undeclared peanut protein.

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

Class II — Potential Health HazardOngoing
Refund
FoodMarch 9, 2015· Cuisine Innovations LLC dba Bon Appetizers, LLC

Recalled Item: Southwestern 4oz Veggie Burger 36 count Net Wt 9 lb. Recalled by Cuisine...

The Issue: Products may contain cumin which may contain undeclared peanut protein.

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

Class II — Potential Health HazardOngoing
Refund
FoodMarch 9, 2015· Cuisine Innovations LLC dba Bon Appetizers, LLC

Recalled Item: Guiltless Gourmet Southwestern Veggie Burger 2.5oz 48 pieces Distributed by:...

The Issue: Products may contain cumin which may contain undeclared peanut protein.

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

Class II — Potential Health HazardOngoing
Refund
FoodMarch 9, 2015· Cuisine Innovations LLC dba Bon Appetizers, LLC

Recalled Item: Chef's Line Black Bean Burger 36-4.25 oz Net Wt. 9 Recalled by Cuisine...

The Issue: Products may contain cumin which may contain undeclared peanut protein.

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

Class II — Potential Health HazardOngoing
Refund
FoodMarch 6, 2015· James G. Cole, Inc., dba ASN/Maxam Neutraceutics

Recalled Item: ALL ASN products: The ASN products are in capsule or Recalled by James G....

The Issue: All ASN brand products are recalled because it was ordered by the United...

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

Class II — Potential Health HazardOngoing
Refund
FoodMarch 6, 2015· James G. Cole, Inc., dba ASN/Maxam Neutraceutics

Recalled Item: ALL MAXAM PRODUCTS: The Maxam product is used orally in Recalled by James G....

The Issue: All Maxam brand products are recalled because it was ordered by the United...

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

Class II — Potential Health HazardOngoing
Refund
FoodMarch 6, 2015· Cost Plus Management Services, Inc.

Recalled Item: Shanghai Ceramic Spoons Recalled by Cost Plus Management Services, Inc. Due...

The Issue: Some ceramic spoons may exceed FDA guidance levels for leachable lead and...

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

Class II — Potential Health HazardOngoing
Refund
Medical DeviceMarch 6, 2015· Wright Medical Technology, Inc.

Recalled Item: CROSSCHECK(R) Plating system Recalled by Wright Medical Technology, Inc. Due...

The Issue: The minor diameter, major diameter, thread pitch, and pitch on the...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 6, 2015· Wright Medical Technology, Inc.

Recalled Item: CROSSCHECK(R) Plating system Recalled by Wright Medical Technology, Inc. Due...

The Issue: The minor diameter, major diameter, thread pitch, and pitch on the...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 6, 2015· Philips Medical Systems (Cleveland) Inc

Recalled Item: Gemini 16 PET/CT System (Uninterruptible Power Supply (UPS) accessory...

The Issue: The firm was notified that the failure of the UPS accessory devices used in...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 6, 2015· Philips Medical Systems (Cleveland) Inc

Recalled Item: Gemini LXL 16 Slice (Uninterruptible Power Supply (UPS) accessory devices)...

The Issue: The firm was notified that the failure of the UPS accessory devices used in...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 6, 2015· Philips Medical Systems (Cleveland) Inc

Recalled Item: MX 16 Slice (Uninterruptible Power Supply (UPS) accessory devices) Computed...

The Issue: The firm was notified that the failure of the UPS accessory devices used in...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 6, 2015· Philips Medical Systems (Cleveland) Inc

Recalled Item: MX 16 Slice Phase II (Uninterruptible Power Supply (UPS) accessory Recalled...

The Issue: The firm was notified that the failure of the UPS accessory devices used in...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 6, 2015· Philips Medical Systems (Cleveland) Inc

Recalled Item: GEMINI TF PET/CT 64 Slice (Uninterruptible Power Supply (UPS) accessory...

The Issue: The firm was notified that the failure of the UPS accessory devices used in...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 6, 2015· Philips Medical Systems (Cleveland) Inc

Recalled Item: iCT SP (Uninterruptible Power Supply (UPS) accessory devices) Computed...

The Issue: The firm was notified that the failure of the UPS accessory devices used in...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 6, 2015· Philips Medical Systems (Cleveland) Inc

Recalled Item: GEMINI TF Big Bore (Uninterruptible Power Supply (UPS) accessory devices)...

The Issue: The firm was notified that the failure of the UPS accessory devices used in...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 6, 2015· Philips Medical Systems (Cleveland) Inc

Recalled Item: Ingenuity PET/MR (Uninterruptible Power Supply (UPS) accessory devices)...

The Issue: The firm was notified that the failure of the UPS accessory devices used in...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 6, 2015· Philips Medical Systems (Cleveland) Inc

Recalled Item: Brilliance CT 6 Slice Air (Uninterruptible Power Supply (UPS) accessory...

The Issue: The firm was notified that the failure of the UPS accessory devices used in...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 6, 2015· Philips Medical Systems (Cleveland) Inc

Recalled Item: Ingenuity Flex (Uninterruptible Power Supply (UPS) accessory devices)...

The Issue: The firm was notified that the failure of the UPS accessory devices used in...

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

Class II — Potential Health HazardOngoing