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. 2,584 recalls have been distributed to District of Columbia in the last 12 months.

47,654 total recalls
2,584 in last 12 months

Showing 1398114000 of 47,654 recalls

Medical DeviceNovember 2, 2021· Cardinal Health

Recalled Item: SmartSleeve Poly-Reinforced Breathable Sleeve Surgical Gowns X-large...

The Issue: Potential for open packaging seals compromising the sterility of the...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 2, 2021· Cardinal Health

Recalled Item: SmartSleeve Poly-Reinforced Breathable Sleeve Surgical Gowns-X-Large SKU:...

The Issue: Potential for open packaging seals compromising the sterility of the...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 2, 2021· Cardinal Health

Recalled Item: Cardinal Health Poly-Reinforced Surgical Gowns Large SKU: 9010 Recalled by...

The Issue: Potential for open packaging seals compromising the sterility of the...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 2, 2021· Cardinal Health

Recalled Item: SmartSleeve Poly-Reinforced Breathable Sleeve Surgical Gowns-Large SKU: 9011...

The Issue: Potential for open packaging seals compromising the sterility of the...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 2, 2021· Cardinal Health

Recalled Item: RoyalSilk Non-Reinforced Surgical Gowns XX-large SKU: 9578 Recalled by...

The Issue: Potential for open packaging seals compromising the sterility of the...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 2, 2021· Cardinal Health

Recalled Item: Cardinal Health Poly-Reinforced Surgical Gowns XX-large SKU: 9070 Recalled...

The Issue: Potential for open packaging seals compromising the sterility of the...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 2, 2021· Cardinal Health

Recalled Item: SmartGown Breathable Surgical Gowns with raglan sleeves X-large Recalled by...

The Issue: Potential for open packaging seals compromising the sterility of the...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 2, 2021· Cardinal Health

Recalled Item: Cardinal Health Poly-Reinforced Surgical Gowns X-large SKU: 9040 Recalled by...

The Issue: Potential for open packaging seals compromising the sterility of the...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 2, 2021· Cardinal Health

Recalled Item: RoyalSilk Non-Reinforced Surgical Gowns XXX-large Recalled by Cardinal...

The Issue: Potential for open packaging seals compromising the sterility of the...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 2, 2021· Magnolia Medical Technologies, Inc.

Recalled Item: The Steripath Gen2 Blood Collection System Model Number/Description...

The Issue: Due to an uptick of complaints associated with premature needle retraction...

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

Class II — Potential Health HazardOngoing
DrugNovember 1, 2021· Precision Dose Inc.

Recalled Item: Acetaminophen Oral Suspension Recalled by Precision Dose Inc. Due to cGMP...

The Issue: cGMP Deviations: Product manufactured with contaminated raw ingredient.

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

Class II — Potential Health HazardOngoing
Refund
DrugNovember 1, 2021· Precision Dose Inc.

Recalled Item: Acetaminophen Oral Suspension Recalled by Precision Dose Inc. Due to cGMP...

The Issue: cGMP Deviations: Product manufactured with contaminated raw ingredient.

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

Class II — Potential Health HazardOngoing
Refund
Medical DeviceNovember 1, 2021· Human Care USA, Inc.

Recalled Item: Hanger-Bar 2P 45cm Recalled by Human Care USA, Inc. Due to The Hanger-Bar is...

The Issue: The Hanger-Bar is being recalled due to the potential for the set screw...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 1, 2021· Human Care USA, Inc.

Recalled Item: Hanger-Bar 2P 45cm Recalled by Human Care USA, Inc. Due to The Hanger-Bar is...

The Issue: The Hanger-Bar is being recalled due to the potential for the set screw...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 1, 2021· Smith & Nephew, Inc.

Recalled Item: smith&Nephew EVOS MEDIAL DISTAL FEMUR PLATE Recalled by Smith & Nephew, Inc....

The Issue: Testing vendor notified Smith & Nephew that previous MRI scanning conditions...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 1, 2021· Smith & Nephew, Inc.

Recalled Item: smith&nephew EVOS CONDYLAR MEDIAL DISTAL FEMUR PLATE Recalled by Smith &...

The Issue: Testing vendor notified Smith & Nephew that previous MRI scanning conditions...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 1, 2021· Smith & Nephew, Inc.

Recalled Item: smith&nephew EVOS CONDYLAR MEDIAL DISTAL FEMUR PLATE Recalled by Smith &...

The Issue: Testing vendor notified Smith & Nephew that previous MRI scanning conditions...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 1, 2021· Smith & Nephew, Inc.

Recalled Item: smith&nephew EVOS MEDIAL DISTAL FEMUR PLATE Recalled by Smith & Nephew, Inc....

The Issue: Testing vendor notified Smith & Nephew that previous MRI scanning conditions...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 1, 2021· Randox Laboratories Ltd.

Recalled Item: RANDOX CHOL-cholesterol (total) test system intended to measure cholesterol...

The Issue: When calibrating using the standard provided in the kit, the change in...

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

Class II — Potential Health HazardOngoing
FoodOctober 31, 2021· Flowers Foods (Corporate Offices)

Recalled Item: Tastykake Butterscotch Krimpets 24oz (12-2ct) Recalled by Flowers Foods...

The Issue: The firm was notified by an ingredient supplier of the potential small metal...

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

Class II — Potential Health HazardOngoing
Refund