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.
Showing 37141–37160 of 47,654 recalls
Recalled Item: New Punjab Kaju (Kajoo) Fry is the Indian translation for Recalled by New...
The Issue: This voluntary recall is being initiated because the following Indian snack...
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: New Punjab Kaju Roll is an Indian snack cut into Recalled by New Punjab...
The Issue: This voluntary recall is being initiated because the following Indian snack...
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: New Punjab Kaju Katri is an Indian snack cut into Recalled by New Punjab...
The Issue: This voluntary recall is being initiated because the following Indian snack...
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: New Punjab Chum Chum is a oval-shaped Indian snack coated Recalled by New...
The Issue: This voluntary recall is being initiated because the following Indian snack...
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: New Punjab Burfi is an Indian snack cut into 1lb Recalled by New Punjab...
The Issue: This voluntary recall is being initiated because the following Indian snack...
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: New Punjab Rosgula is a ball-shaped Indian snack. Product is Recalled by New...
The Issue: This voluntary recall is being initiated because the following Indian snack...
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: New Punjab Ladoo is a ball-shaped Indian snack coated with Recalled by New...
The Issue: This voluntary recall is being initiated because the following Indian snack...
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: UBERVITA LOSE WEIGHT FAST W700 THERMOGENIC HYPER-METABOLIZER DIETARY...
The Issue: It has come to the attention of Ubervita LLC that a packaging error has...
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Primus (THE BTE WS30) Recalled by BTE Technologies, Inc. Due to On the...
The Issue: On the Primus that includes the optional Chop / Lift Bar, there is a remote...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Spinal Elements 5.5 x 45MM Mercury lordosed rod. A component Recalled by...
The Issue: Some rods may not meet the appropriate traceability requirements including...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: TFN-ADVANCED Proximal Femoral Nailing System (TFNA) Recalled by Synthes,...
The Issue: TFNA nails from certain lots were assembled with a locking mechanism too...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: BARD MAX-CORE Disposable Core Biopsy Instrument Gauge x Length 18g Recalled...
The Issue: The firm is recalling Bard MAX-CORE Disposable Core Biopsy Instrument due to...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Genesis Malleable Penile Prosthesis Recalled by Coloplast Manufacturing US,...
The Issue: Several lots of the 9.5 mm Genesis Malleable Penile Prosthesis were...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ABACUS SE (Single-Workstation Edition) and ABACUS ME (Multi-Workstation...
The Issue: Baxter Corporation is conducting a field action for the ABACUS SE and ME...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Hydroxyzine Hydrochloride Recalled by Akorn, Inc. Due to Failed...
The Issue: Failed Impurities/Degradation Specifications
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Hydroxyzine Hydrochloride Recalled by Akorn, Inc. Due to Failed...
The Issue: Failed Impurities/Degradation Specifications
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Olanzapine Recalled by Apotex Inc. Due to Subpotent drug
The Issue: Subpotent drug
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Olanzapine Recalled by Apotex Inc. Due to Subpotent drug
The Issue: Subpotent drug
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Olanzapine Recalled by Apotex Inc. Due to Subpotent drug
The Issue: Subpotent drug
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: 0.9% Sodium Chloride Injection Recalled by Hospira Inc. Due to Lack of...
The Issue: Lack of Sterility Assurance: The product has the potential to leak at the...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.