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. 2,515 recalls have been distributed to Maine in the last 12 months.
Showing 11921–11940 of 48,770 recalls
Recalled Item: JIF 1.5 oz CRUNCHY PEANUT BUTTER TO GO packaged in 8 count cases Recalled by...
The Issue: Products are potentially contaminated with Salmonella.
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: JIF CRUNCHY PEANUT BUTTER packaged in 500 gram Recalled by The JM Smucker...
The Issue: Products are potentially contaminated with Salmonella.
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: JIF NATURAL CREAMY PEANUT BUTTER packaged in 16oz Recalled by The JM Smucker...
The Issue: Products are potentially contaminated with Salmonella.
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: JIF DARK ROAST CREMY PEANUT BUTTER packaged in 500 gram and 1 kilogram...
The Issue: Products are potentially contaminated with Salmonella.
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: JIF 1.5 oz NATURAL CREAMY PEANUT BUTTER TO GO packaged in 8 and 36 count...
The Issue: Products are potentially contaminated with Salmonella.
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: JIF 16 OUNCE NATURAL CREAMY PEANUT BUTTER HONEY Recalled by The JM Smucker...
The Issue: Products are potentially contaminated with Salmonella.
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: EIT CIF cage Recalled by DePuy Spine, Inc. Due to Label on the Outer Carton...
The Issue: Label on the Outer Carton does not match the labels on the Outer Blister...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: regard Item Number: 800774001 Recalled by ROi CPS LLC Due to A nonsterile...
The Issue: A nonsterile component was packaged in a sterile convenience kit.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Kit Label: Anti-FITC-AP CISH Accessory Kit (Dako Omnis) Recalled by Agilent...
The Issue: Label provided for substrate vail contained incorrect expiration date.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: PALMAZ GENESIS Transhepatic Biliary Stent on OPTA PRO .035" Delivery System...
The Issue: Potential for stent dislodgement and associated failures related to two...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: EIT CIF cage Recalled by DePuy Spine, Inc. Due to Label on the Outer Carton...
The Issue: Label on the Outer Carton does not match the labels on the Outer Blister...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Sensica Urine Output System Recalled by C.R. Bard Inc Due to Complaints...
The Issue: Complaints relating to urine output measurement accuracy.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Rocuronium Bromide Injection Recalled by Nephron Sterile Compounding Center...
The Issue: Lack of Assurance of Sterility
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Fentanyl Citrate in 0.9% Sodium Chloride Injection Recalled by Nephron...
The Issue: Lack of Assurance of Sterility
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Oxytocin 30 Units/500 mL (0.06 Units/mL) in 0.9% Sodium Chloride Injection...
The Issue: Lack of Assurance of Sterility
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Alprostadil Injection USP 500 mcg/mL Recalled by Teva Pharmaceuticals USA...
The Issue: Failed Impurities/Degradation Specifications; out-of-specification results...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Phenylephrine HCl Injection Recalled by Nephron Sterile Compounding Center...
The Issue: Lack of Assurance of Sterility
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Losartan Potassium Tablets Recalled by Strides Pharma Inc. Due to CGMP...
The Issue: CGMP Deviations- AZIDO Impurity levels observed to be above acceptable limits
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Phenylephrine HCl Injection Recalled by Nephron Sterile Compounding Center...
The Issue: Lack of Assurance of Sterility
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Calcium Gluconate Injection Recalled by Nephron Sterile Compounding Center...
The Issue: Lack of Assurance of Sterility
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.