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. 1,099 recalls have been distributed to Delaware in the last 12 months.
Showing 1281–1300 of 48,330 recalls
Recalled Item: EVIS EXERA BRONCHOVIDEOSCOPE OLYMPUS BF TYPE XT160 Recalled by Olympus...
The Issue: Additional IFU updates to provide further clarification on safe and...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Harris Teeter CINNAMON TEXAS TOAST Recalled by Harris Teeter Due to...
The Issue: Undeclared Milk. During production the firm discovered that the ingredients...
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: EVIS EXERA III BRONCHOVIDEOSCOPE OLYMPUS BF-1TH190 Recalled by Olympus...
The Issue: Additional IFU updates to provide further clarification on safe and...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Harris Teeter ASIAGO TEXAS TOAST Recalled by Harris Teeter Due to Undeclared...
The Issue: Undeclared Milk. During production the firm discovered that the ingredients...
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: iNSitu Bipolar Hip System Recalled by Theken Companies LLC Due to Downstream...
The Issue: Downstream recall for RES 97605, BioPro femoral components. Product failed...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: EVIS EXERA II BRONCHOVIDEOSCOPE OLYMPUS BF TYPE 1TQ180 Recalled by Olympus...
The Issue: Additional IFU updates to provide further clarification on safe and...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: The failure occurs if a user on the Omnipod 5 Recalled by Insulet...
The Issue: The failure occurs if a user on the Omnipod 5 iOS application selects and...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: EVIS EXERA III BRONCHOVIDEOSCOPE OLYMPUS BF-P190 Recalled by Olympus...
The Issue: Additional IFU updates to provide further clarification on safe and...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: CXR Preconnect with TENACIO Pump with InhibiZone Recalled by Boston...
The Issue: The potential for devices to experience inflation and/or deflation...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: CX Preconnect with TENACIO Pump without InhibiZone Recalled by Boston...
The Issue: The potential for devices to experience inflation and/or deflation...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: BRONCHOVIDEOSCOPE OLYMPUS BF-H1100 Recalled by Olympus Corporation of the...
The Issue: Additional IFU updates to provide further clarification on safe and...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: EVIS EXERA b BRONCHOVIDEOSCOPE OLYMPUS BF-XT190 Recalled by Olympus...
The Issue: Additional IFU updates to provide further clarification on safe and...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: BRONCHOFIBERSCOPE OLYMPUS BF TYPE TE2 Recalled by Olympus Corporation of the...
The Issue: Additional IFU updates to provide further clarification on safe and...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: BRONCHOVIDEOSCOPE OLYMPUS BF TYPE 1T150 Recalled by Olympus Corporation of...
The Issue: Additional IFU updates to provide further clarification on safe and...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: EVIS EXERA III BRONCHOVIDEOSCOPE OLYMPUS BF-Q190 Recalled by Olympus...
The Issue: Additional IFU updates to provide further clarification on safe and...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: EVIS EXERA II BRONCHOVIDEOSCOPE OLYMPUS BF TYPE P180 Recalled by Olympus...
The Issue: Additional IFU updates to provide further clarification on safe and...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: LGX Preconnect with TENACIO Pump without InhibiZone Recalled by Boston...
The Issue: The potential for devices to experience inflation and/or deflation...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: TENACIO Pump with InhibiZone Recalled by Boston Scientific Corporation Due...
The Issue: The potential for devices to experience inflation and/or deflation...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: BRONCHOFIBERSCOPE OLYMPUS BF TYPE PE2 Recalled by Olympus Corporation of the...
The Issue: Additional IFU updates to provide further clarification on safe and...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: BRONCHOVIDEOSCOPE OLYMPUS BF-1TQ170 Recalled by Olympus Corporation of the...
The Issue: Additional IFU updates to provide further clarification on safe and...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.