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. 1,069 recalls have been distributed to Delaware in the last 12 months.
Showing 9881–9900 of 27,373 recalls
Recalled Item: DEXCOM G6 SENSOR 3 PACK Item Number: 5447552 Recalled by Cardinal Health...
The Issue: Due to shipping delays the devices were exposed to temperature excursions of...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ONETOUCH ULTRA BLUE TEST STRIPS 100 COUNT Item Number: 2990174 Recalled by...
The Issue: Due to shipping delays the devices were exposed to temperature excursions of...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: VAPORIZER VICKS 1.5GAL Item Number: 2354942 Recalled by Cardinal Health Inc....
The Issue: Due to shipping delays the devices were exposed to temperature excursions of...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ONETOUCH DELICA LANCETS 30G 100 COUNT Item Number: 5541610 Recalled by...
The Issue: Due to shipping delays the devices were exposed to temperature excursions of...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: BD UF PEN 32GX4MM 100 NANO Item Number: 4292272 Recalled by Cardinal Health...
The Issue: Due to shipping delays the devices were exposed to temperature excursions of...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ONETOUCH ULTRA TEST STRIPS 25 COUNT Item Number: 3510443 Recalled by...
The Issue: Due to shipping delays the devices were exposed to temperature excursions of...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: AEROCHAMBER PLS W/MASK LRG BLU Item Number: 1496033 Recalled by Cardinal...
The Issue: Due to shipping delays the devices were exposed to temperature excursions of...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: FREESTYLE LANCETS 28G 100CT Item Number:2975670 Recalled by Cardinal Health...
The Issue: Due to shipping delays the devices were exposed to temperature excursions of...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ONETOUCH DELICA LANCETS 33G 100 COUNT Item Number: 5541628 Recalled by...
The Issue: Due to shipping delays the devices were exposed to temperature excursions of...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ONETOUCH ULTRASOFT LANCETS 100 COUNT Item Number: 3007788 Recalled by...
The Issue: Due to shipping delays the devices were exposed to temperature excursions of...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: VIDAS¿ CMV IgM 30 Tests Recalled by Biomerieux Inc Due to bioMerieux...
The Issue: bioMerieux received complaints about calibration issue observed on several...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ENDURITY Pulse Generator **** SN ********* St. Jude Medical Recalled by St....
The Issue: Due to a manufacturing issue associated with the mixing process of the epoxy...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Filtered Triple-Leg Extension Set - Intravascular administration set....
The Issue: BBMI has identified through complaints the potential for the extension set...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ASSURITY Pulse Generator **** SN ********* ST. JUDE MEDICAL Recalled by St....
The Issue: Due to a manufacturing issue associated with the mixing process of the epoxy...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Diluent Recalled by Medline Industries Inc Due to Possible false negative or...
The Issue: Possible false negative or false positive results due to the product being...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: HydraVision Digital Imaging System Product ID/Reorder Number: 705559 (65KW)...
The Issue: Failure to comply with the performance standard for fluoroscopy systems. Per...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Tritanium X TL Instruments - intervertebral fusion device with bone graft...
The Issue: Stryker identified non-conforming instruments that are components of the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Tibial Opening Wedge Osteotomy Plate Recalled by Arthrex, Inc. Due to It was...
The Issue: It was discovered that five AR-13200ST-15.0 parts were processed as...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Ysio X.pree Recalled by Siemens Medical Solutions USA, Inc Due to A patient...
The Issue: A patient image was assigned to a different patient during image recovery...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: AngioDynamics SafeSheath ULTRALITE 10F Recalled by Oscor, Inc. Due to...
The Issue: Potential for open seal on sterile product
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.