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. 2,395 recalls have been distributed to District of Columbia in the last 12 months.

47,654 total recalls
2,395 in last 12 months

Showing 4280142820 of 47,654 recalls

DrugAugust 6, 2013· Teva Pharmaceuticals USA, Inc.

Recalled Item: Propranolol Hydrochloride Tablets Recalled by Teva Pharmaceuticals USA, Inc....

The Issue: Failed Tablet/Capsule Specification: Teva is recalling certain lots of...

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

Class II — Potential Health HazardOngoing
Refund
DrugAugust 6, 2013· Novartis Consumer Health

Recalled Item: Maalox Nighttime Antacid with Acid Barrier (calcium carbonate and Recalled...

The Issue: Labeling: Incorrect Or Missing Lot and/or Exp Date: The lot number and/or...

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

Class III — Low RiskOngoing
Refund
DrugAugust 6, 2013· Novartis Consumer Health

Recalled Item: Maalox Extra Strength Antacid with Anti-Gas (calcium carbonate and...

The Issue: Labeling: Incorrect Or Missing Lot and/or Exp Date: The lot number and/or...

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

Class III — Low RiskOngoing
Refund
DrugAugust 6, 2013· Novartis Consumer Health

Recalled Item: Maalox Extra Strength Antacid (calcium carbonate) chewable tablets Recalled...

The Issue: Labeling: Incorrect Or Missing Lot and/or Exp Date: The lot number and/or...

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

Class III — Low RiskOngoing
Refund
DrugAugust 6, 2013· Novartis Consumer Health

Recalled Item: Maalox Recalled by Novartis Consumer Health Due to Labeling: Incorrect Or...

The Issue: Labeling: Incorrect Or Missing Lot and/or Exp Date: The lot number and/or...

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

Class III — Low RiskOngoing
Refund
DrugAugust 6, 2013· Novartis Consumer Health

Recalled Item: Maalox Nighttime Antacid with Acid Barrier (calcium carbonate and Recalled...

The Issue: Labeling: Incorrect or Missing Lot and/or Exp Date: The lot number and/or...

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

Class III — Low RiskOngoing
Refund
DrugAugust 6, 2013· Novartis Consumer Health

Recalled Item: Maalox Regular Strength Antacid (calcium carbonate) chewable tablets...

The Issue: Labeling: Incorrect Or Missing Lot and/or Exp Date: The lot number and/or...

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

Class III — Low RiskOngoing
Refund
DrugAugust 6, 2013· Novartis Consumer Health

Recalled Item: Maalox Advanced Maximum Strength Antacid & Antigas (calcium carbonate and...

The Issue: Labeling: Incorrect Or Missing Lot and/or Exp Date: The lot number and/or...

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

Class III — Low RiskOngoing
Refund
DrugAugust 6, 2013· Novartis Consumer Health

Recalled Item: Maalox Extra Strength Antacid with Anti-Gas (calcium carbonate and...

The Issue: Labeling: Incorrect Or Missing Lot and/or Exp Date: The lot number and/or...

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

Class III — Low RiskOngoing
Refund
DrugAugust 6, 2013· Showline Automotive Products, Inc. dba US Soaps Mfg. Company

Recalled Item: REEVA (triclosan) Antibacterial Hand Soap and Dishwashing Liquid Recalled by...

The Issue: Microbial Contamination of a Non-Sterile Products: Product was found to be...

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

Class II — Potential Health HazardOngoing
Refund
DrugAugust 6, 2013· Novartis Consumer Health

Recalled Item: Maalox Advanced Maximum Strength Antacid & Antigas (calcium carbonate and...

The Issue: Labeling: Incorrect Or Missing Lot and/or Exp Date: The lot number and/or...

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

Class III — Low RiskOngoing
Refund
FoodAugust 6, 2013· Novartis Consumer Health

Recalled Item: Benefiber Recalled by Novartis Consumer Health Due to The lot number and/or...

The Issue: The lot number and/or expiration date may be illegible on the outer plastic...

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

Class III — Low RiskOngoing
Refund
FoodAugust 6, 2013· Novartis Consumer Health

Recalled Item: Benefiber Recalled by Novartis Consumer Health Due to The lot number and/or...

The Issue: The lot number and/or expiration date may be illegible on the outer plastic...

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

Class III — Low RiskOngoing
Refund
FoodAugust 6, 2013· Novartis Consumer Health

Recalled Item: Benefiber Recalled by Novartis Consumer Health Due to The lot number and/or...

The Issue: The lot number and/or expiration date may be illegible on the outer plastic...

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

Class III — Low RiskOngoing
Refund
FoodAugust 6, 2013· Novartis Consumer Health

Recalled Item: Benefibre Recalled by Novartis Consumer Health Due to The lot number and/or...

The Issue: The lot number and/or expiration date may be illegible on the outer plastic...

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

Class III — Low RiskOngoing
Refund
FoodAugust 6, 2013· Novartis Consumer Health

Recalled Item: Benefiber Recalled by Novartis Consumer Health Due to The lot number and/or...

The Issue: The lot number and/or expiration date may be illegible on the outer plastic...

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

Class III — Low RiskOngoing
Refund
Medical DeviceAugust 6, 2013· Smith & Nephew, Inc. Endoscopy Division

Recalled Item: OSTEORAPTOR 2.3 mm Suture Anchor with 1 ULTRABRAID COBRAID Suture Recalled...

The Issue: Pinholes detected in a small number of primary pouches that may constitute a...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 6, 2013· Smith & Nephew, Inc. Endoscopy Division

Recalled Item: OSTEORAPTOR 2.9 mm Suture Anchor with 2 ULTRABRAID Suture Recalled by Smith...

The Issue: Pinholes detected in a small number of primary pouches that may constitute a...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 6, 2013· Smith & Nephew, Inc. Endoscopy Division

Recalled Item: OSTEORAPTOR 2.9 mm Suture Anchor with 1 ULTRABRAID Suture Recalled by Smith...

The Issue: Pinholes detected in a small number of primary pouches that may constitute a...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 6, 2013· Smith & Nephew, Inc. Endoscopy Division

Recalled Item: BIORAPTOR 2.9 mm Suture Anchor Straight Recalled by Smith & Nephew, Inc....

The Issue: Pinholes detected in a small number of primary pouches that may constitute a...

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

Class II — Potential Health HazardOngoing