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. 2,395 recalls have been distributed to District of Columbia in the last 12 months.
Showing 41801–41820 of 47,654 recalls
Recalled Item: Siemens SOMATOM Definition Recalled by Siemens Medical Solutions USA, Inc...
The Issue: During clinical operation, a malfunction may occur causing a system display...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: GE Healthcare Innova IGS 630. Biplane Cardiovascular and Interventional...
The Issue: GE Healthcare has recently become aware of a potential safety issue with...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: HemosIL High Abnormal Control 3 UNASSAYED Part Number: 0020003320 Recalled...
The Issue: HemosIL Low, Abnormal, Normal Controls UNASSAYED (no-value assigned) lacks...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Mega Needle Driver Recalled by Intuitive Surgical, Inc. Due to Firm has...
The Issue: Firm has become aware of the potential for detachment of the jaw insert for...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: HemosIL Normal Control 1 UNASSAYED Part Number: 0020003120 Recalled by...
The Issue: HemosIL Low, Abnormal, Normal Controls UNASSAYED (no-value assigned) lacks...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Large Needle Driver Recalled by Intuitive Surgical, Inc. Due to Firm has...
The Issue: Firm has become aware of the potential for detachment of the jaw insert for...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Fluconazole Oral Suspension Recalled by Teva Pharmaceuticals USA, Inc. Due...
The Issue: Failed Stability Specifications: this product is below specification for...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Renasys EZ PLUS Recalled by Smith & Nephew Inc. Due to Modification of the...
The Issue: Modification of the bacterial overflow guard (filter) and related changes to...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Renasys EZ Recalled by Smith & Nephew Inc. Due to Modification of the...
The Issue: Modification of the bacterial overflow guard (filter) and related changes to...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: VerifyNow IIb/IIIa Test Recalled by Accumetrics Inc Due to Accumetrics is...
The Issue: Accumetrics is recalling the VerifyNow IIb/IIIa 10-Test because it contains...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Namenda XR (memantine HCl) Recalled by Forest Pharmaceuticals Inc Due to...
The Issue: Failed Dissolution Specifications: Three lots of product being recalled...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Namenda XR (memantine HCl) Recalled by Forest Pharmaceuticals Inc Due to...
The Issue: Failed Dissolution Specifications: Three lots of product being recalled...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Namenda XR (memantine HCl) Recalled by Forest Pharmaceuticals Inc Due to...
The Issue: Failed Dissolution Specifications: Three lots of product being recalled...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Gluten Free 60 vcaps Recalled by Mrm Due to Metabolic Response Modifier...
The Issue: Metabolic Response Modifier (MRM) is recalling Gluten Free 60 vcaps because...
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: RTC 25-C Inline Aerosol Tee Adapter. Intended to be used Recalled by...
The Issue: Some packages of the RTC 25-C may have been shipped to customers with...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Broncho Flexible Fiberscope Recalled by Karl Storz Endoscopy America Inc Due...
The Issue: KARL STORZ Endoscopy America, Inc. is recalling the Flexible Broncho...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Intubation Flexible Fiberscope Recalled by Karl Storz Endoscopy America Inc...
The Issue: KARL STORZ Endoscopy America, Inc. is recalling the Flexible Broncho...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: 10% Recalled by Baxter Healthcare Corp. Due to Lack of Assurance of...
The Issue: Lack of Assurance of Sterility; Drug product leaking from container...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Innate Response Digestive Enzymes Clinical Strength 90ct. (40126) and "...
The Issue: Potential for Chloramphenicol contamination.
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: MegaFood Vegan-Ease 30 ct. (12002) and MegaFood Vegan-Ease 2 ct. Recalled by...
The Issue: Potential for Chloramphenicol contamination.
Recommended Action: Do not consume. Return to store for a refund or discard.