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. 2,674 recalls have been distributed to Delaware in the last 12 months.
Showing 4621–4640 of 27,373 recalls
Recalled Item: Access Total T4 Recalled by Beckman Coulter, Inc. Due to Four lots of Access...
The Issue: Four lots of Access Total T4 reagent lots demonstrated imprecision outside...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: microStar Reader Recalled by Landauer Due to Permanent discontinuance of the...
The Issue: Permanent discontinuance of the microSTARii medical dosimetry system....
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: CLEARLINK Non-DEHP Solution Set Luer Lock Adapter Recalled by Baxter...
The Issue: Baxter Healthcare Corporation is issuing an Urgent Medical Device Recall for...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Torrent Suite Dx Software versions 5.14 and earlier used in Recalled by Life...
The Issue: Torrent Suite Dx Software versions 5.14 and earlier used in connection with...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Access Substrate Recalled by Beckman Coulter, Inc. Due to On 07 February...
The Issue: On 07 February 2024 Beckman Coulter made the decision to conduct a field...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: TENSIVE Conductive Adhesive Gel Recalled by Natus Neurology Inc Due to Natus...
The Issue: Natus has become aware that its third-party supplier Parker Laboratories...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: smiths medical Pneupac paraPAC plus 310 ventilator kit with PEEP and CPAP...
The Issue: When a paraPAC plus ventilator is switched to the operating mode of...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: smiths medical Pneupac paraPAC plus 300 ventilator kit without PEEP and CPAP...
The Issue: When a paraPAC plus ventilator is switched to the operating mode of...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: natus neurology Recalled by Natus Neurology Inc Due to Natus has become...
The Issue: Natus has become aware that its third-party supplier Parker Laboratories...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: DCA Systems HbA1c Reagent Kit Recalled by Siemens Healthcare Diagnostics,...
The Issue: The reason for the recall is that the Siemens DCA HbA1c Reagent Kit was...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: SPII Model Lubinus Recalled by Waldemar Link GmbH & Co. KG (Mfg Site) Due to...
The Issue: Due to two complaints, has come to our attention that additional guidance is...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: SPII Model Lubinus Recalled by Waldemar Link GmbH & Co. KG (Mfg Site) Due to...
The Issue: Due to two complaints, has come to our attention that additional guidance is...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: SPII Model Lubinus Recalled by Waldemar Link GmbH & Co. KG (Mfg Site) Due to...
The Issue: Due to two complaints, has come to our attention that additional guidance is...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: SPII Model Lubinus Recalled by Waldemar Link GmbH & Co. KG (Mfg Site) Due to...
The Issue: Due to two complaints, has come to our attention that additional guidance is...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: NO 4 TRIATHLON TS PLUS TIB INS X3 POLY 16 MM Recalled by Howmedica Osteonics...
The Issue: Potential packaging breaches of inner blister and outer sterile blister.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: NO 4 TRIATHLON TS PLUS TIB INS X3 POLY 11 MM Recalled by Howmedica Osteonics...
The Issue: Potential packaging breaches of inner blister and outer sterile blister.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: X3 TRIATHLON CS INSERT NO 6 10 MM Recalled by Howmedica Osteonics Corp. Due...
The Issue: Potential packaging breaches of inner blister and outer sterile blister.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: X3 TRIATHLON CS INSERT NO 3 10 MM Recalled by Howmedica Osteonics Corp. Due...
The Issue: Potential packaging breaches of inner blister and outer sterile blister.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: NO 3 TRIATHLON TS PLUS TIB INS X3 POLY 11 MM Recalled by Howmedica Osteonics...
The Issue: Potential packaging breaches of inner blister and outer sterile blister.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: X3 TRIATHLON CS INSERT NO 7 9 MM Recalled by Howmedica Osteonics Corp. Due...
The Issue: Potential packaging breaches of inner blister and outer sterile blister.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.