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.
Showing 8161–8180 of 47,654 recalls
Recalled Item: Norepinephrine 8 mg per 250 mL (32 mcg per mL) in 0.9% Sodium Chloride...
The Issue: Lack of Assurance of Sterility
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Norepinephrine 32 mg per 250 mL (128 mcg per mL) in 0.9% Sodium Chloride...
The Issue: Lack of Assurance of Sterility
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Ziyad Brand Jameed Soup Starter sold in a 35.2 fluid Recalled by ZB...
The Issue: Does not declare the major food allergen "milk"
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Five S 5 3x65 Recalled by Karl Storz Endoscopy Due to Flexible intubation...
The Issue: Flexible intubation endoscopes sterility assurance can not be confirmed.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: LIF AMP Recalled by Alphatec Spine, Inc. Due to Awl instrument adjustable...
The Issue: Awl instrument adjustable drill button assembly assembled in the incorrect...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Betty Lou's Paleo Java Nuts About Energy Balls with Cacao Recalled by Betty...
The Issue: Undeclared sesame. Paleo Java Nuts About Energy Balls with Cacao, Coffee &...
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: APK2 Pressure-Sensing Wheelchair Cushions Recalled by Aquila Corporation Due...
The Issue: Defective battery pack in wheelchair cushions can overheat resulting in...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: SofTech Pressure-Sensing Wheelchair Cushions Recalled by Aquila Corporation...
The Issue: Defective battery pack in wheelchair cushions can overheat resulting in...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Loteprednol Etabonate Ophthalmic Suspension Recalled by SUN PHARMACEUTICAL...
The Issue: Superpotent Drug: Out of Specification (OOS) results observed for unit dose...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Sunitinib Malate Capsules Recalled by Teva Pharmaceuticals USA Inc Due to...
The Issue: Failed Moisture Limits: Water (moisture) content above the approved product...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: 0.9% Sodium Chloride Injection USP Recalled by B. Braun Medical Inc. Due to...
The Issue: Lack of assurance of sterility: bags have the potential to leak.
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Bivalirudin for Injection 250 mg Recalled by Accord Healthcare, Inc. Due to...
The Issue: Presence of Particulate Matter: Particulate matter identified as fiber.
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Atropine Sulfate Injection Recalled by Accord Healthcare, Inc. Due to...
The Issue: Presence of Particulate Matter: Particulate matter identified as fiber.
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: LINK MP Monoblock Hip Stem Recalled by Waldemar Link GmbH & Co. KG (Mfg...
The Issue: Increased force may be required to remove the LINK MP Monoblock trial hip...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: LINK MP Monoblock Hip Stem Recalled by Waldemar Link GmbH & Co. KG (Mfg...
The Issue: Increased force may be required to remove the LINK MP Monoblock trial hip...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: LINK MP Monoblock Hip Stem Recalled by Waldemar Link GmbH & Co. KG (Mfg...
The Issue: Increased force may be required to remove the LINK MP Monoblock trial hip...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Total Hip Kit Recalled by MEDLINE INDUSTRIES, LP - Northfield Due to The...
The Issue: The prep solution included in the Total Hip Kit expires prior to the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: LINK MP Monoblock Hip Stem Recalled by Waldemar Link GmbH & Co. KG (Mfg...
The Issue: Increased force may be required to remove the LINK MP Monoblock trial hip...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: LINK MP Monoblock Hip Stem Recalled by Waldemar Link GmbH & Co. KG (Mfg...
The Issue: Increased force may be required to remove the LINK MP Monoblock trial hip...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: LINK MP Monoblock Hip Stem Recalled by Waldemar Link GmbH & Co. KG (Mfg...
The Issue: Increased force may be required to remove the LINK MP Monoblock trial hip...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.