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. 1,050 recalls have been distributed to Delaware in the last 12 months.
Showing 11261–11280 of 48,330 recalls
Recalled Item: Mrs. Freshley's Apple Fruit Pie NET WT 4.5 OZ (128g) Recalled by Flowers...
The Issue: During an internal inspection the firm discovered that several products may...
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: TASTYKAKE GLAZED CARAMEL APPLE PIE NET WT 4.5 OZ (128g) Recalled by Flowers...
The Issue: During an internal inspection the firm discovered that several products may...
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Rifampin Capsules Recalled by Golden State Medical Supply Inc. Due to Failed...
The Issue: Failed impurities/degradation specifications: Finished product exceeds the 5...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Rifampin Capsules Recalled by Golden State Medical Supply Inc. Due to Failed...
The Issue: Failed impurities/degradation specifications: Finished product exceeds the 5...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Fogarty Arterial Embolectomy Catheters Model Number: 120602FP 120403FP...
The Issue: Due to an increase of confirmed latex deterioration complaints for arterial...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Fogarty Biliary Balloon Probes Model Number: 410235FP 410405FP 410236FP...
The Issue: Due to an increase of confirmed latex deterioration complaints for arterial...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Quinapril and Hydrochlorothiazide Tablets Recalled by Aurobindo Pharma USA...
The Issue: CGMP Deviations: Detection of N-Nitroso-quinapril impurity above the...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: 8.4% Sodium Bicarbonate Injection Recalled by Exela Pharma Sciences LLC Due...
The Issue: Defective Container: Complaints received of vial breakage and glass flying...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: 8.4% Sodium Bicarbonate Injection Recalled by Exela Pharma Sciences LLC Due...
The Issue: Defective Container: Complaints received of vial breakage and glass flying...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: MicroScan autoSCAN-4 Instrument Recalled by Beckman Coulter, Inc. Due to Due...
The Issue: Due to MicroScan autoSCAN-4 Instruments being manufactured with an incorrect...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Blinq Pediatric Vision Scanner-Pediatric Vision Scanner-intended for...
The Issue: Unable to charge the battery pack- battery packs will allow the batteries to...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: BD Multitest 6-Color TBNK with optional BD Trucount Tubes (Cat. No. 662995)...
The Issue: Due to partial label detachment on tubes. This can cause tubes to become...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: BD Trucount Tubes (Cat. No. 340334) Recalled by Becton, Dickinson and...
The Issue: Due to partial label detachment on tubes. This can cause tubes to become...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: BD Trucount Tubes (Cat. No. 663028) Recalled by Becton, Dickinson and...
The Issue: Due to partial label detachment on tubes. This can cause tubes to become...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: MEDLINE RADIOLOGY PROCEDURE PACK Recalled by MEDLINE INDUSTRIES, LP -...
The Issue: Medline received complaints on some of the breather pouches with in the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: BAUSCH + LOMB EYE PACK Recalled by MEDLINE INDUSTRIES, LP - Northfield Due...
The Issue: Medline received complaints on some of the breather pouches with in the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: MEDLINE LINQ TRAY Recalled by MEDLINE INDUSTRIES, LP - Northfield Due to...
The Issue: Medline received complaints on some of the breather pouches with in the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: MEDLINE DENTAL PACK Recalled by MEDLINE INDUSTRIES, LP - Northfield Due to...
The Issue: Medline received complaints on some of the breather pouches with in the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: EMBLEM MRI S-ICD Recalled by Boston Scientific Corporation Due to There is...
The Issue: There is an incorrect manufacturing date/timestamp within the software which...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Stryker INBONE Tibial Tray Recalled by Wright Medical Technology, Inc. Due...
The Issue: The tibial tray lock detail is oversized (larger than specification).
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.