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. 904 recalls have been distributed to Delaware in the last 12 months.
Showing 47181–47200 of 48,330 recalls
Recalled Item: Kleenex Luxury Foam Hand Sanitizer Recalled by Kimberly-Clark Corporation...
The Issue: Microbial Contamination of Non-Sterile Products; The affected lots were...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: ZEE Antiseptic Wipes Recalled by Dukal Corp. Due to Microbial contamination...
The Issue: Microbial contamination of Non Sterile Product; contamination with...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Kleenex Foam Hand Sanitizer Recalled by Kimberly-Clark Corporation Due to...
The Issue: Microbial Contamination of Non-Sterile Products; The affected lots were...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Dukal Corporation BZK Swab Recalled by Dukal Corp. Due to Microbial...
The Issue: Microbial contamination of Non Sterile Product; contamination with...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: seprafilm¿ Procedure Pack ADHESION BARRIER Re-order Number: 5086-02 Product...
The Issue: Sterility of product may be compromised due to packaging defect
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: seprafilm¿ Single Site ADHESION BARRIER Re-order Number: 6641-01 Product...
The Issue: Sterility of product may be compromised due to packaging defect
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: GE Healthcare Recalled by GE Healthcare, LLC Due to GE has become aware of...
The Issue: GE has become aware of multiple issues affecting the Dash 3000/4000/5000 and...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: GE Healthcare Recalled by GE Healthcare, LLC Due to GE has become aware of...
The Issue: GE has become aware of multiple issues affecting the Dash 3000/4000/5000...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Ocean Manna Korean IQF Oysters Recalled by Pacific Giant, Inc Due to Pacific...
The Issue: Pacific Giant is recalling all frozen (IQF) oyster meat and 1/2 shell...
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: FF Cream of Crab Soup 3109 Net Weight 4-4 LB. Recalled by Winter Gardens...
The Issue: Possible processing temperature issue that occurred during the production of...
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Maryland Style Crab Soup 2340 Net Weight 4-4LBS. Winter Garden Quality Foods...
The Issue: Possible processing temperature issue that occurred during the production of...
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Lobster Bisque 3107 Net Weight 4-4 LBS. Keep Packed Recalled by Winter...
The Issue: Possible processing temperature issue that occurred during the production of...
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: New England Clam Chowder 2338 Net Weight 4-4LBS. KEEP Recalled by Winter...
The Issue: Possible processing temperature issue that occurred during the production of...
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: GE Healthcare Recalled by GE Healthcare, LLC Due to GE Healthcare has become...
The Issue: GE Healthcare has become aware through complaints of a potential safety...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: QUADROX iD HMOD 2030 Diffusion Membrane Oxygenator Recalled by Maquet...
The Issue: It has come to firm's attention that, in some rare cases, the blood outlet...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Hudson RCI Concha Therm Neptune Humidifier Recalled by Teleflex Medical Due...
The Issue: Speaker Failure. If the speaker fails and an event occurs which would...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Carestream DRX-1 System Battery --- Made in U.S.A. for Carestream Health...
The Issue: Carestream DRX-1 System batteries manufactured before June 2012 due to two...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Sterile Distraction Screws of 3 different sizes: 12mm Recalled by Tedan...
The Issue: This letter is to notify you that several of our sterile screw products are...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Fertalin bottles of 90 tablets taken orally Nokomis Research Inc Recalled by...
The Issue: The products contain synthetic equivalents of spermine and/or spermidine,...
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Product Name: Eroxil bottles of 30 tablets taken orally Nokomis Research Inc...
The Issue: The products contain synthetic equivalents of spermine and/or spermidine,...
Recommended Action: Do not consume. Return to store for a refund or discard.