Product Recalls in Maryland
Product recalls affecting Maryland — including food, drugs, consumer products, medical devices, and vehicles distributed to Maryland. RecallDetector monitors distribution data from the FDA, USDA, CPSC, and NHTSA to show you which recalls are relevant to your area. 2,597 recalls have been distributed to Maryland in the last 12 months.
Showing 1381–1400 of 52,535 recalls
Recalled Item: OES BRONCHOFIBERSCOPE OLYMPUS BF TYPE MP60 Recalled by Olympus Corporation...
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-Q170 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: OES BRONCHOFIBERSCOPE OLYMPUS BF TYPE XT40 Recalled by Olympus Corporation...
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-H190 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-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: OES BRONCHOFIBERSCOPE OLYMPUS BF TYPE 1T60 Recalled by Olympus Corporation...
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: 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: 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: GOODLES VEGAN IS BELIEVIN' PLANT-BASED WHITE CHEDDAR WITH SPIRALS NET...
The Issue: Undeclared allergens (milk).
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: GOODLES HERE COMES TRUFFLE CREAMY TRUFFLE FLAVORED CHEDDAR AND SHELLS...
The Issue: Undeclared allergens (cashews).
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Medline Adult Anesthesia Set Recalled by Medline Industries, LP Due to...
The Issue: Specific items and lots of Medline Kits may contain Clearlink IV Sets which...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Ashvins variant HEYEX 2 / HEYEX PACS. Software Version: Version Recalled by...
The Issue: Potential that the measured value may be smaller than the actual area.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Juggerknot Mini Soft Anchors Recalled by Biomet, Inc. Due to The outer...
The Issue: The outer carton box label is for the JuggerKnot 1.0mm Mini products....
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ICU Medical ChemoLock Port Recalled by ICU Medical, Inc. Due to Port weld of...
The Issue: Port weld of drug transfer device may separate or break during use and...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ICU Medical Oncology Kit w/2 ChemoLock" Recalled by ICU Medical, Inc. Due to...
The Issue: Port weld of drug transfer device may separate or break during use and...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ICU Medical Double ChemoLock Port Syringe Transfer Set Recalled by ICU...
The Issue: Port weld of drug transfer device may separate or break during use and...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ICU Medical ChemosafeLock Bag Spike Recalled by ICU Medical, Inc. Due to...
The Issue: Port weld of drug transfer device may separate or break during use and...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ICU Medical 45" (114 cm) Appx 1.7 ml Recalled by ICU Medical, Inc. Due to...
The Issue: Port weld of drug transfer device may separate or break during use and...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.