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. 2,366 recalls have been distributed to District of Columbia in the last 12 months.
Showing 45021–45040 of 47,654 recalls
Recalled Item: Stelkast Cross-over Acetabular Shell and Liner Hip System Recalled by...
The Issue: Firm was made aware of incidents relating to the difficulty of properly...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: D3000I Advantage Drive System Recalled by Linvatec Corp. dba ConMed Linvatec...
The Issue: The Membrane Switch Panel ( to as "front panel" of the component part number...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: D3000 Advantage Drive System Recalled by Linvatec Corp. dba ConMed Linvatec...
The Issue: The Membrane Switch Panel ( to as "front panel" of the component part number...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Sodium Sulfacetamide 10% and Sulfur 5% Lotion Recalled by Mission Pharmacal...
The Issue: Superpotent: Drug product active ingredients were formulated incorrectly...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Terazosin Hydrochloride Capsules Recalled by Teva Pharmaceuticals USA, Inc....
The Issue: Presence of Foreign Tablets/Capsules: Recall is being conducted due to a...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Crest PRO-HEALTH CPC Antigingivitis/Antiplaque Oral Rinse Recalled by...
The Issue: Cross Contamination with Other Products: Product was mixed with another type...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Plastic bottle containing 3.5 mL of IgG FITC Conjugate Product Recalled by...
The Issue: Affected products have a labeled expiration date of one year too long.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: BARD Biopsy Systems (A Business Unit of Bard Peripheral Vascular Recalled by...
The Issue: Bard Peripheral Vascular (BPV) is initiating this recall because a...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: MICROSHEATH¿ - 0.066 (1.7mm) proximal Recalled by Bard Peripheral Vascular...
The Issue: Bard Peripheral Vascular (BPV) is initiating this recall because a...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: USHER¿ Support Catheter- Angled Tip WL130cm Recalled by Bard Peripheral...
The Issue: Bard Peripheral Vascular (BPV) is initiating this recall because a...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: BARD Biopsy Systems (A Business Unit of Bard Peripheral Vascular Recalled by...
The Issue: Bard Peripheral Vascular (BPV) is initiating this recall because a...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Plastic bottle containing 10.5 mL of IgG Conjugate Product Usage: Recalled...
The Issue: Affected products have a labeled expiration date of one year too long.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Plastic bottle containing 10.5 mL of IgM Conjugate Product Usage: Recalled...
The Issue: Affected products have a labeled expiration date of one year too long.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: IRINOTECAN HYDROCHLORIDE INJECTION Recalled by Fresenius Kabi USA LLC (FK...
The Issue: Crystallization: Active pharmaceutical ingredient is precipitating in...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Medi-bolic Booster Injectable (methionine 8.3 mg/mL Recalled by RX South LLC...
The Issue: CGMP Deviations: Pharmaceutical for injection was not manufactured according...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Syeda (drospirenone and ethinyl estradiol) Recalled by Sandoz Incorporated...
The Issue: Tablet/Capsule Imprinted with Wrong ID; a portion of the tablets could...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Cardinal Health hCG Cassette Rapid Test Recalled by Alere San Diego, Inc....
The Issue: Alere San Diego Inc. is recalling the Cardinal Health hCG Cassette Rapid...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: GE Healthcare Advantx Recalled by GE Healthcare, LLC Due to A locking nut...
The Issue: A locking nut might loosen out of the overhead Video Monitor Suspension yoke...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Lifeguard Infusion Set with Smartsite Recalled by Churchill Medical Systems,...
The Issue: The label on the device states that the item number is CLGY-2210 when the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Pamela's Chocolate Cake Mix Recalled by Pamela's Products, Inc. Due to Firm...
The Issue: Firm received complaints for on four (4) products which may contain glass or...
Recommended Action: Do not consume. Return to store for a refund or discard.