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. 960 recalls have been distributed to Delaware in the last 12 months.
Showing 33801–33820 of 48,330 recalls
Recalled Item: Ultra 8 IAB: 8Fr 40cc Recalled by Arrow International, Inc., Division of...
The Issue: The sheath body may become separated from the sheath hub. If the separation...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: RediGuard IAB: 7Fr 30cc Recalled by Arrow International, Inc., Division of...
The Issue: The sheath body may become separated from the sheath hub. If the separation...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: UltraFlex IAB: 7.5Fr 30cc Recalled by Arrow International, Inc., Division of...
The Issue: The sheath body may become separated from the sheath hub. If the separation...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: FiberOptix Ultra 8 IAB: 8Fr 30cc The Arrow¿ IAB is Recalled by Arrow...
The Issue: The sheath body may become separated from the sheath hub. If the separation...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: eValueMed Infant Transport Mattress 301-1015 Recalled by Philips Electronics...
The Issue: eValueMed Infant Heel Warmers and eValueMed Infant Transport Mattresses bear...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Simplexa Group A Strep Direct (MOL2850) with Direct Amplification Disc...
The Issue: Focus Diagnostics is recalling the Direct Amplification Discs (DAD) supplied...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Simplexa HSV 1&2 Direct (MOL2150) with Direct Amplification Disc (MOL1451...
The Issue: Focus Diagnostics is recalling the Direct Amplification Discs (DAD) supplied...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Simplexa Flu A/B & RSV Direct (MOL2650) with Direct Amplification Disc...
The Issue: Focus Diagnostics is recalling the Direct Amplification Discs (DAD) supplied...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: evaluemed Infant Heel Warmer 301-1223 Recalled by Philips Electronics North...
The Issue: eValueMed Infant Heel Warmers and eValueMed Infant Transport Mattresses bear...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: RayStation Therapy Treatment Planning System Stand-alone Software 3.0...
The Issue: A software issue with editing tools that use the left mouse button held...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Adult Robitussin PEAK COLD Cough & Chest Congestion DM Liquid Recalled by...
The Issue: Labeling: Label Mix-Up
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: TEARS Naturale FREE (dextran 70 and hypromellose 2910) lubricant eye drops...
The Issue: Lack of Assurance of Sterility: Some single-use vials may be filled with...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Denali Filter-Femoral Delivery System Product Code: DL900F/DL950F Recalled...
The Issue: Bard Peripheral Vascular, Inc. is recalling Denali Filter-Jugular/Subclavian...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Denali Filter-Jugular/Subclavian Delivery System Product Code: DL900J/DL950J...
The Issue: Bard Peripheral Vascular, Inc. is recalling Denali Filter-Jugular/Subclavian...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Deer Cumin Powder 7 oz.. Recalled by Best Foods NJ, Inc. Due to Undeclared...
The Issue: Cumin may contain undeclared peanut.
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Merge Cardio software. The firm name on the label is Merge Healthcare...
The Issue: A report can be confirmed with the incorrect patient demographics resulting...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: MicroAire PAL-R4011XL - 40cm x 4 mm Del Vecchio French Rasp aspiration...
The Issue: Complaints that the cannula bent/broke during surgery.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: MicroAire PAL¿ Cannula Product Usage - Power Aspiration Device Recalled by...
The Issue: MicroAire has initiated a recall on product PAL-R4011XL (40cm x 4mm Del...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: TF Adaptive Gutta Percha Point Size SM3 50pk Recalled by Ormco/Sybronendo...
The Issue: Ormco Corporation is recalling the TF Adaptive Gutta Percha Point Size...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Medicated Better Braids Recalled by Keystone Laboratories Inc Due to...
The Issue: Microbial Contamination of a Non-Sterile Products: The product had a...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.