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. 997 recalls have been distributed to Delaware in the last 12 months.
Showing 18041–18060 of 48,330 recalls
Recalled Item: 54 IN (137 cm) APPX 7.2 ml EXT SET w NanoClave 4-Way Stopcock Recalled by...
The Issue: Identification of a potential manufacturing defect on the internal surface...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: 5.5" (14 cm) Appx 0.39 ml Recalled by ICU Medical, Inc. Due to...
The Issue: Identification of a potential manufacturing defect on the internal surface...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: 11 IN(28cm)APPX 0.97ml Recalled by ICU Medical, Inc. Due to Identification...
The Issue: Identification of a potential manufacturing defect on the internal surface...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: 112 IN(284cm) APPX 14.6ml Recalled by ICU Medical, Inc. Due to...
The Issue: Identification of a potential manufacturing defect on the internal surface...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: 7" (18 cm) Appx 0.32 ml Recalled by ICU Medical, Inc. Due to Identification...
The Issue: Identification of a potential manufacturing defect on the internal surface...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: 10 IN (25cm) APPX 1.5ml EXT w/6-Port NanoClave Manifold Recalled by ICU...
The Issue: Identification of a potential manufacturing defect on the internal surface...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: 128" (325 cm) Appx 16.6 ml Recalled by ICU Medical, Inc. Due to...
The Issue: Identification of a potential manufacturing defect on the internal surface...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Clonazepam Orally Disintegrating Tablets Recalled by SUN PHARMACEUTICAL...
The Issue: Cross contamination with other products - OOS discovered during routine...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Skin Medica Acne System Recalled by Allergan PLC Due to SUBPOTENT DRUG:...
The Issue: SUBPOTENT DRUG: Products failed assay results at the 12 and 24 month timepoints.
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Skin Medica Acne Treatment Lotion (Benzoyl Peroxide 2.5%) Recalled by...
The Issue: SUBPOTENT DRUG: Products failed assay results at the 12 and 24 month timepoints.
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: DYNEX Agility Recalled by Dynex Technologies, Inc. Due to Control samples...
The Issue: Control samples aspirated from wrong SmartKit on the Agility. Agility...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Metformin Hydrochloride Extended-Release Tablets USP Recalled by Granules...
The Issue: CGMP Deviations: FDA analysis detected N-Nitrosodimethylamine (NDMA)...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Tadalafil 26 mg Capsule Recalled by MasterPharm LLC Due to Lack of...
The Issue: Lack of Processing Controls (lack of assurance of conformity to specifications).
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Vardenafil 20 mg Troche Recalled by MasterPharm LLC Due to Lack of...
The Issue: Lack of Processing Controls (lack of assurance of conformity to specifications).
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Estriol 8 mg Capsule Recalled by MasterPharm LLC Due to Lack of Processing...
The Issue: Lack of Processing Controls (lack of assurance of conformity to specifications).
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Cefdinir for Oral Suspension USP Recalled by Lupin Pharmaceuticals Inc. Due...
The Issue: Superpotent Drug: Out-of-specification (OOS) result observed in an assay...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: bio aaa Advance Hand Sanitizer Ethyl Alcohol 70% Recalled by AAA Cosmetica,...
The Issue: CGMP Deviations
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: bio aaa Advance Hand Sanitizer Ethyl Alcohol 70% Recalled by AAA Cosmetica,...
The Issue: Chemical Contamination: Product contains methanol.
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Formula 82M (Minoxidil 5%/Tretinoin 0.01%/Fluocinolone acetonide 0.01%)...
The Issue: Lack of Processing Controls (lack of assurance of conformity to specifications).
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Progesterone 150 mg Troche Recalled by MasterPharm LLC Due to Lack of...
The Issue: Lack of Processing Controls (lack of assurance of conformity to specifications).
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.