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. 2,392 recalls have been distributed to Maine in the last 12 months.
Showing 22301–22320 of 48,770 recalls
Recalled Item: Atropine 0.01% Eye Drops Recalled by Anderson Compounding Pharmacy, Inc. DBA...
The Issue: Lack of sterility assurance.
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Prostaglandin Tri-Mix 30:30:1 Injection Recalled by Anderson Compounding...
The Issue: Lack of sterility assurance.
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Serum Tears 30% Drops Recalled by Anderson Compounding Pharmacy, Inc. DBA...
The Issue: Lack of sterility assurance.
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Penicillin G 100 Recalled by Anderson Compounding Pharmacy, Inc. DBA...
The Issue: Lack of sterility assurance.
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Testosterone Cypionate 250 mg/mL Sterile Injection Recalled by Anderson...
The Issue: Lack of sterility assurance.
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Prostaglandin Tri-Mix 8.33:22.5:0.833 Injection Recalled by Anderson...
The Issue: Lack of sterility assurance.
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Polyhexamethylene Biguanide 0.02% Ophthalmic Drops Recalled by Anderson...
The Issue: Lack of sterility assurance.
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Phenylephrine 1 mg/mL Injection Recalled by Anderson Compounding Pharmacy,...
The Issue: Lack of sterility assurance.
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: HCG 20 Day Extra Strength Recalled by Anderson Compounding Pharmacy, Inc....
The Issue: Lack of sterility assurance.
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Prostaglandin Quad-Mix 20:30:1:0.15 Injection Recalled by Anderson...
The Issue: Lack of sterility assurance.
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Phenol 10% Injection Recalled by Anderson Compounding Pharmacy, Inc. DBA...
The Issue: Lack of sterility assurance.
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Prostaglandin Tri-Mix 50:30:1 Recalled by Anderson Compounding Pharmacy,...
The Issue: Lack of sterility assurance.
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Olympus MAJ-209 Single Use Suction Valves Recalled by Olympus Corporation of...
The Issue: There is a potential for the single use suction valve to come apart and/or...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Mobi-C 14mm Distraction Screw Recalled by Zimmer Biomet, Inc. Due to...
The Issue: Incorrect part description contained on an additional label placed on the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: RUSCH LASERTUBE (Rubber) Recalled by Teleflex Medical Due to The firm...
The Issue: The firm received reports indicating that the laser guard foil partially...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: RUSCH LASERTUBE (Rubber) Recalled by Teleflex Medical Due to The firm...
The Issue: The firm received reports indicating that the laser guard foil partially...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: RUSCH LASERTUBE (Rubber) Recalled by Teleflex Medical Due to The firm...
The Issue: The firm received reports indicating that the laser guard foil partially...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: RUSCH LASERTUBE (Rubber) Recalled by Teleflex Medical Due to The firm...
The Issue: The firm received reports indicating that the laser guard foil partially...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: RUSCH LASERTUBE (Rubber) Recalled by Teleflex Medical Due to The firm...
The Issue: The firm received reports indicating that the laser guard foil partially...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Dornier Diode Laser Fibers:Used with Dornier Medilas D Family Lasers...
The Issue: Pin hole package failures compromising sterility of product
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.