Product Recalls in Delaware
Product recalls affecting Delaware — including food, drugs, consumer products, medical devices, and vehicles distributed to Delaware. RecallDetector monitors distribution data from the FDA, USDA, CPSC, and NHTSA to show you which recalls are relevant to your area. 2,668 recalls have been distributed to Delaware in the last 12 months.
Showing 5821–5840 of 48,330 recalls
Recalled Item: Clorazepate Dipotassium Tablets Recalled by Aurobindo Pharma USA Inc. Due to...
The Issue: Discoloration: Dotted and yellow spots on tablets
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Sodium Sulfacetamide 10% - Sulfur 5% Cleanser Recalled by Acella...
The Issue: Subpotent drug
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: EasySuite 4K Integrated Operating Room System Model/Catalog Number:...
The Issue: A subset of the ES4K systems do not have complete records for earth leakage...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Brand Name: EsophaCap Product Name: EsophaCap (25mm diameter Recalled by...
The Issue: The EsophaCap sponge may be at increased risk of detaching from the string...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Brand Name: EsophaCap Product Name: EsophaCap (20mm diameter Recalled by...
The Issue: The EsophaCap sponge may be at increased risk of detaching from the string...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: EYLEA Recalled by Regeneron Pharmaceuticals Inc Due to Lack of Assurance of...
The Issue: Lack of Assurance of Sterility: Complaints of syringe breakage
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: minolira (minocycline hydrochloride) extended-release tablets Recalled by...
The Issue: CGMP Deviation: Discontinuation of the Quality program by manufacturer that...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Cloderm (clocortolone pivalate) Cream Recalled by EPI Health, LLC Due to...
The Issue: CGMP Deviation: Discontinuation of the Quality program by manufacturer that...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: minolira (minocycline hydrochloride) extended-release tablets Recalled by...
The Issue: CGMP Deviation: Discontinuation of the Quality program by manufacturer that...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Coviden Monoject 60ml Syringe Luer-Lock Tip-used to inject fluid into...
The Issue: Quarantined product was inadvertently distributed
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Trevo ProVue Recalled by Stryker Neurovascular Due to Neurovascular devices...
The Issue: Neurovascular devices did not meet the minimum sample size required for...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Trevo Trak 21 Microcatheter Recalled by Stryker Neurovascular Due to...
The Issue: Neurovascular devices did not meet the minimum sample size required for...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Synchro .014"guide wire Recalled by Stryker Neurovascular Due to...
The Issue: Neurovascular devices did not meet the minimum sample size required for...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: DAC 044 115cm Recalled by Stryker Neurovascular Due to Neurovascular devices...
The Issue: Neurovascular devices did not meet the minimum sample size required for...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Trevo NXT ProVue 3 x 32 Recalled by Stryker Neurovascular Due to...
The Issue: Neurovascular devices did not meet the minimum sample size required for...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Trevo XP ProVue Retriever 4 x 20 Recalled by Stryker Neurovascular Due to...
The Issue: Neurovascular devices did not meet the minimum sample size required for...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: FlowGate2 8F x 85cm Recalled by Stryker Neurovascular Due to Neurovascular...
The Issue: Neurovascular devices did not meet the minimum sample size required for...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Trevo Pro 14 Microcatheter Recalled by Stryker Neurovascular Due to...
The Issue: Neurovascular devices did not meet the minimum sample size required for...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Cascade IOMAX Cortical Module Recalled by Cadwell Industries Inc Due to...
The Issue: There is the potential that an electroneurodiagnostic medical device...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: SURGIFOAM" Absorbable Gelatin Powder Kit Recalled by Ethicon, Inc. Due to...
The Issue: Some applicator tips from these lots had open seals.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.