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. 2,655 recalls have been distributed to Delaware in the last 12 months.
Showing 7881–7900 of 48,330 recalls
Recalled Item: EMPOWR Acetabular System Recalled by Encore Medical, LP Due to Knee insert...
The Issue: Knee insert and acetabular system parts were swapped within inner pack prior...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: EMPOWR 3D Knee Tibial Insert Recalled by Encore Medical, LP Due to Knee...
The Issue: Knee insert and acetabular system parts were swapped within inner pack prior...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Apellis Injection Kit 29g Injection Needle -single use intended to Recalled...
The Issue: 19-gauge x 1" inch filter needles showed appearances of a small fraction of...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: therascreen ¿KRAS RGQ PCR Kit (24)-IVD qualitative PCR assay used Recalled...
The Issue: Handbook Revision (Rev13) a dilution step is indicated as an Action when...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Palindrome Chronic Catheter Kit Symmetrical Tip14.5 Fr/Ch(4.8mm)x23cm...
The Issue: Some catheter kits labeled as 23 cm implant length incorrectly included...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: 3M Attest Super Rapid Readout Biological Indicator Recalled by 3M Company -...
The Issue: Specific lots of 3M Attest Super Rapid Readout Biological Indicators...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: 3M Attest Super Rapid 5 Steam-Plus Steam Challenge Pack Recalled by 3M...
The Issue: Specific lots of 3M Attest Super Rapid Readout Biological Indicators...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: 3M Attest Super Rapid Readout Steam Challenge Pack Recalled by 3M Company -...
The Issue: Specific lots of 3M Attest Super Rapid Readout Biological Indicators...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: 3M Attest Super Rapid 5 Steam-Plus Steam Challenge Pack Recalled by 3M...
The Issue: Specific lots of 3M Attest Super Rapid Readout Biological Indicators...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Humanrace Suncare Recalled by HUMANRACE Due to Subpotent Drug: Product does...
The Issue: Subpotent Drug: Product does not contain SPF that is declared on the label.
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Humanrace Suncare Recalled by HUMANRACE Due to Subpotent Drug: Product does...
The Issue: Subpotent Drug: Product does not contain SPF that is declared on the label.
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Individually Quick Frozen (IQF) Corn Recalled by Twin City Foods, Inc. Due...
The Issue: Listeria monocytogenes
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Mixed Vegetables BEST PRICE TOPVALU Recalled by Twin City Foods, Inc. Due to...
The Issue: Listeria monocytogenes
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Kernel Corn Recalled by Twin City Foods, Inc. Due to Potential Listeria...
The Issue: Listeria monocytogenes
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Individually Quick Frozen (IQF) Corn distributed in BULK TOTES (1650lbs...
The Issue: Listeria monocytogenes
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: OPMI LUMERA 300 Recalled by Carl Zeiss Suzhou Co., Ltd. Due to Surgical...
The Issue: Surgical microscope for use in ophthalmology may be missing a screw from the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: CARDIOPLEGIA SOLUTION Recalled by Central Admixture Pharmacy Services, Inc....
The Issue: Lack of Assurance of Sterility:Lack of validation data for sanitization cycles
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: dilTIAZem 125mg/125mL (1 mg/mL) Recalled by Central Admixture Pharmacy...
The Issue: Lack of Assurance of Sterility:Lack of validation data for sanitization cycles
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Cardioplegia Solution Recalled by Central Admixture Pharmacy Services, Inc....
The Issue: Lack of Assurance of Sterility:Lack of validation data for sanitization cycles
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: EPINEPHrine added to 0.9% sodium chloride Recalled by Central Admixture...
The Issue: Lack of Assurance of Sterility:Lack of validation data for sanitization cycles
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.