Product Recalls in Maine
Product recalls affecting Maine — including food, drugs, consumer products, medical devices, and vehicles distributed to Maine. RecallDetector monitors distribution data from the FDA, USDA, CPSC, and NHTSA to show you which recalls are relevant to your area. 2,317 recalls have been distributed to Maine in the last 12 months.
Showing 38721–38740 of 48,770 recalls
Recalled Item: Dried Bean Curd Anka Flavor 24x150g Recalled by Gemini Food Corporation Inc...
The Issue: Gemini Foods is recalling bean curd products because they may be...
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Dried Bean Curd Spicy Flavor 24x150g Recalled by Gemini Food Corporation Inc...
The Issue: Gemini Foods is recalling bean curd products because they may be...
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Roland brand Bruschetta Recalled by American Roland Food Corp. Due to Glass...
The Issue: Glass fragment found in product.
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Perfect Bar Peanut Butter Recalled by Perfect Foods Bar Due to Potential...
The Issue: Perfect Bar is recalling Peanut Butter and Cranberry Crunch nutritional bars...
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Perfect Bar Variety Pack (Costco Only) Recalled by Perfect Foods Bar Due to...
The Issue: Perfect Bar is recalling Peanut Butter and Cranberry Crunch nutritional bars...
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Perfect Bar Cranberry Crunch Recalled by Perfect Foods Bar Due to Potential...
The Issue: Perfect Bar is recalling Peanut Butter and Cranberry Crunch nutritional bars...
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Sweet Blueberry Almonds - Blueberry Flavored Almonds. Ingredients: Almonds...
The Issue: Inspector at manufacturing facility noticed that product label did not...
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Philips IntelliVue Information Center iX (release A.00 Recalled by Philips...
The Issue: Sp02 and/or Non Invasive Blood Pressure (NBP) alarms may become disabled...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Synthes Electric Pen Drive (EPD) System Recalled by Synthes, Inc. Due to In...
The Issue: In May 2013, the original recall was initiated due to complaints the Hand...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Focal Sim radiation therapy treatment planning system Recalled by Elekta,...
The Issue: Incorrect CT to ED when using the Monaco Image Statistics Tool.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Monaco radiation therapy treatment planning system. The Monaco system is...
The Issue: Incorrect CT to ED when using the Monaco Image Statistics Tool.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: The MAYFIELD¿ Ultra 360 Base Unit for head positioner Recalled by Integra...
The Issue: Through an investigation of complaints, Integra found that there is the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: BD 10 mL Syringe BD Luer-Lok Tip with Blunt Plastic Cannula Recalled by...
The Issue: The stopper of the 10mL BD Luer-Lok syringe is not properly seated in the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: LINAC Accelerators: ARTISTE Recalled by Siemens Medical Solutions USA, Inc...
The Issue: A hardware update to replace the old PCB Assembly, Head Driver-G41 with PCB...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Quickie Q7 Adult Rigid Wheelchair Model EIR4. Recalled by Sunrise Medical...
The Issue: There is the potential for the height adjustable handle to dislodge due to...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: HEPFLUSH-10 (HEPARIN LOCK FLUSH SOLUTION Recalled by Fresenius Kabi USA, LLC...
The Issue: The lot failed pH specification.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Zippie Zone Pediatric Rigid Wheelchair Model EIRZ1. Recalled by Sunrise...
The Issue: There is the potential for the height adjustable handle to dislodge due to...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: CD8 (Leu-2a) PE (In vitro diagnostic) Recalled by BD Biosciences, Systems &...
The Issue: One lot of CD8 PE is contaminated with CD4 FITC and may cause an unexpected...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Anti-Lambda APC-H7 Recalled by BD Biosciences, Systems & Reagents Due to Two...
The Issue: Two lots of the Anti-Lambda APC-H7 antibody are contaminated with CD38 antibody.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: lnline Persuader- PedFuse Pedicle Screw System Recalled by SpineFrontier,...
The Issue: A crack may develop in the handle to the Inline Persuader, which may...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.