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. 2,616 recalls have been distributed to District of Columbia in the last 12 months.

47,654 total recalls
2,616 in last 12 months

Showing 85418560 of 47,654 recalls

Medical DeviceMay 23, 2023· TEI Biosciences, Inc.

Recalled Item: SurgiMend PRS Meshed Recalled by TEI Biosciences, Inc. Due to Possible out...

The Issue: Possible out of specification endotoxin test results due to issues with...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 23, 2023· TEI Biosciences, Inc.

Recalled Item: SurgiMend 3.0 Recalled by TEI Biosciences, Inc. Due to Possible out of...

The Issue: Possible out of specification endotoxin test results due to issues with...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 23, 2023· TEI Biosciences, Inc.

Recalled Item: SurgiMend 1.0 Recalled by TEI Biosciences, Inc. Due to Possible out of...

The Issue: Possible out of specification endotoxin test results due to issues with...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 23, 2023· TEI Biosciences, Inc.

Recalled Item: PriMatrix Fenestrated Recalled by TEI Biosciences, Inc. Due to Possible out...

The Issue: Possible out of specification endotoxin test results due to issues with...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 23, 2023· TEI Biosciences, Inc.

Recalled Item: PriMatrix Ag Recalled by TEI Biosciences, Inc. Due to Possible out of...

The Issue: Possible out of specification endotoxin test results due to issues with...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 23, 2023· TEI Biosciences, Inc.

Recalled Item: PriMatrix Recalled by TEI Biosciences, Inc. Due to Possible out of...

The Issue: Possible out of specification endotoxin test results due to issues with...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 23, 2023· TEI Biosciences, Inc.

Recalled Item: PriMatrix Ag Fenestrated Recalled by TEI Biosciences, Inc. Due to Possible...

The Issue: Possible out of specification endotoxin test results due to issues with...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 23, 2023· TEI Biosciences, Inc.

Recalled Item: Revize Recalled by TEI Biosciences, Inc. Due to Possible out of...

The Issue: Possible out of specification endotoxin test results due to issues with...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 23, 2023· TEI Biosciences, Inc.

Recalled Item: Revize-X Recalled by TEI Biosciences, Inc. Due to Possible out of...

The Issue: Possible out of specification endotoxin test results due to issues with...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 23, 2023· TEI Biosciences, Inc.

Recalled Item: SurgiMend MP Recalled by TEI Biosciences, Inc. Due to Possible out of...

The Issue: Possible out of specification endotoxin test results due to issues with...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 23, 2023· TEI Biosciences, Inc.

Recalled Item: SurgiMend Recalled by TEI Biosciences, Inc. Due to Possible out of...

The Issue: Possible out of specification endotoxin test results due to issues with...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 23, 2023· TEI Biosciences, Inc.

Recalled Item: SurgiMend 4.0 Recalled by TEI Biosciences, Inc. Due to Possible out of...

The Issue: Possible out of specification endotoxin test results due to issues with...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 23, 2023· TEI Biosciences, Inc.

Recalled Item: PriMatrix Meshed Recalled by TEI Biosciences, Inc. Due to Possible out of...

The Issue: Possible out of specification endotoxin test results due to issues with...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 23, 2023· TEI Biosciences, Inc.

Recalled Item: SurgiMend 2.0 Recalled by TEI Biosciences, Inc. Due to Possible out of...

The Issue: Possible out of specification endotoxin test results due to issues with...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 23, 2023· TEI Biosciences, Inc.

Recalled Item: TissueMend Recalled by TEI Biosciences, Inc. Due to Possible out of...

The Issue: Possible out of specification endotoxin test results due to issues with...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 23, 2023· TEI Biosciences, Inc.

Recalled Item: SurgiMend PRS Recalled by TEI Biosciences, Inc. Due to Possible out of...

The Issue: Possible out of specification endotoxin test results due to issues with...

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

Class II — Potential Health HazardOngoing
DrugMay 22, 2023· New England Life Care, Inc. dba Advanced Compounding Solutions

Recalled Item: Phenylephrine HCl 20 mg added to 0.9% Sodium Chloride 250mL Bag Recalled by...

The Issue: Product Mix up; Product was compounded in 250 mL 5% Dextrose instead of 250...

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

Class III — Low RiskOngoing
Refund
DrugMay 22, 2023· Aurobindo Pharma USA Inc.

Recalled Item: Pain Reliever Recalled by Aurobindo Pharma USA Inc. Due to Failed...

The Issue: Failed Impurities/Degradation Specifications: firm's investigation due to...

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

Class II — Potential Health HazardOngoing
Refund
FoodMay 22, 2023· Van Leeuwen Ice Cream LLC

Recalled Item: Van Leeuwen brand BROWN SUGAR CHUNK WITH COOKIE DOUGH & BROWNIES FENCH ICE...

The Issue: Product may contain undeclared walnuts.

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

Class I — Serious Health HazardOngoing
Refund
Medical DeviceMay 22, 2023· CareFusion 303, Inc.

Recalled Item: BD Pyxis CII Safe Recalled by CareFusion 303, Inc. Due to Automated...

The Issue: Automated dispensing cabinet devices plugged into any multi-socket outlet...

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

Class II — Potential Health HazardOngoing