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 41521–41540 of 48,770 recalls
Recalled Item: Edwards Lifesciences Fem-Flex II Arterial and femoral Cannulae with Duraflo...
The Issue: Potential for separation of dilator tips.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Tikosyn¿ (dofetilide) 500 mcg (0.5mg) capsules Recalled by Pfizer Inc. Due...
The Issue: Presence of Foriegn Tablets/Capsules: A single Tikosyn¿ (dofetilide) 250 mcg...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: MicroScan Pos Combo Panel Type 33 (PC33): Catalog number B1017-211 Recalled...
The Issue: Siemens investigation confirmed that a portion one lot of panel Pos Combo 33...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: e.cam -emission computed tomography system Used to detect or image Recalled...
The Issue: There is a potential for patient finger injury on the e.cam systems.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Intended for both adult and pediatric patients for taking diagnostic...
The Issue: In special cases, during the start-up of the current model of MobileDiagnost...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: BUPRENORPHINE HYDROCHLORIDE Sublingual Tablets Recalled by Teva...
The Issue: Failed Impurities/Degradation Specifications: High out of specification...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: BUPRENORPHINE HYDROCHLORIDE Sublingual Tablets Recalled by Teva...
The Issue: Failed Impurities/Degradation Specifications: High out of specification...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Sevoflurane Recalled by Piramal Critical Care, Inc. Due to Failed pH...
The Issue: Failed pH Specifications: product was too acidic.
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Natural Grocers by Vitamin Cottage Recalled by Natural Grocers by Vitamin...
The Issue: Vitamin Cottage Natural Food Markets, Inc., a Lakewood, Colorado based...
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Lipase Reagent Recalled by Abbott Laboratories, Inc Due to Package inserts...
The Issue: Package inserts have incorrect SmartWash parameters for Triglyceride.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Model RG3000 and RG4000 Series Valve Integrated Pressure Regulator (VIPR)...
The Issue: Separation events have occurred, including the VIPR separating from the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: SBi RingFix Olive Wires Product Usage: These are temporary devices Recalled...
The Issue: Small Bone Innovations (SBI) is recalling non-sterile RingFIX Olive Wires...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Azathioprine Tablets USP Recalled by Boehringer Ingelheim Roxane Inc Due to...
The Issue: Labeling: Incorrect or Missing Lot and/or Exp Date: This recall is being...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Mercaptopurine Tablets USP Recalled by Boehringer Ingelheim Roxane Inc Due...
The Issue: Labeling: Incorrect or Missing Lot and/or Exp Date: This recall is being...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: 1) Frontier Natural Products Co-op Recalled by Frontier Natural Products...
The Issue: Testing of organic whole black peppercorns revealed the presence of Salmonella
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Lithium Ion Battery M4605A and M4607A for use with IntelliVue Recalled by...
The Issue: The risk of battery failure increases with age, when a battery remains in...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Kit 8551/856X (includes Models 8561 Recalled by Medtronic Neuromodulation...
The Issue: Some kits in the affected lots may contain an extension tubing set that is...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: AMIA v1.0 APD System. For Automated Peritoneal Dialysis (APD) therapy...
The Issue: Additional warning in the AMIA APD System labeling for patients vulnerable...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Medrad Continuum MR Infusion system- non-wireless system The MEDRAD...
The Issue: There is a potential safety risk associated with potentially damaged locking...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Sprotte Spinal Tray / Sprotte Spinal Needle 24 gauge with Recalled by B....
The Issue: B.Braun Medical, Inc. (BBMI) has received reports of 24 gauge Sprotte...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.