Every recall we track for Allergan, PLC. — 26 in all — plus the complaints and injury reports the public filed about them.
Allergan recalls REFRESH Contact Lens Comfort Drops 0.4 fl oz due to missing instruction manual. Consumers should check product details and contact Allergan for guidance.
Allergan is a global leader in medical devices, specializing in innovative products for the healthcare industry. We provide cutting-edge solutions for surgical procedures, diagnostics, and patient care.
Allergan is a global leader in medical devices, specializing in innovative products for surgical procedures, including advanced surgical tools, implants, and medical devices. Their products are used in various medical fields such as plastic surgery, orthopedics, and more.
Allergan, PLC. - Allergan, PLC. - Allergan, PLC.
Allergan, PLC. - Allergan
Allergan recalls XEN Gel Stents with specific lot numbers due to potential residual polishing compounds on the injector needle that could cause eye irritation, inflammation, or allergic reactions during glaucoma treatment.
Allergan recalls textured breast implants due to higher risk of anaplastic large cell lymphoma (BIA-ALCL). Affected implants include RITZ PRINCESS, BIOCELL, INTRASHIEL, and BioDIMENSIONAL styles RML/RMM/RFL/RFM.
Allergan recalls McGhan BioDIMENSIONAL silicone-filled breast implants style 153 due to higher risk of anaplastic large cell lymphoma (BIA-ALCL).
Allergan recalls certain breast implants due to higher risk of anaplastic large cell lymphoma (BIA-ALCL) in textured implants. This recall affects breast augmentation and reconstruction patients.
Allergan recalls Natrelle 410 textured breast implants due to higher risk of BIA-ALCL. Affected models include LL, LM, LF, LX, ML, MM, MF, MX, FL, FM, FF, FX styles. Contact for removal or replacement.
Allergan recalls Natrelle 133 tissue expanders due to higher risk of anaplastic large cell lymphoma (BIA-ALCL) in some patients. Affected models include specific style numbers and UDI codes.
Allergan recalls Natrelle 133 tissue expanders due to higher risk of anaplastic large cell lymphoma (BIA-ALCL) in some patients. Learn which models are affected and what to do.
Allergan recalls certain silicone-filled breast implants due to higher risk of anaplastic large cell lymphoma (BIA-ALCL) in patients with textured implants. Affected products include Natrelle and McGhan brands.
Allergan recalls McGhan Cro:134 tissue expanders after FDA reports higher risk of BIA-ALCL in patients with textured implants. Affected users should contact for return or repair.
Allergan recalls specific silicone breast implants due to increased risk of BIA-ALCL, a rare lymphoma. Affected implants include Natrelle, McGhan, TruForm 2, BIOCELL, and Styles 110/120. No remedy details provided in recall notice.
Allergan recalls Natrelle Inspira textured silicone breast implants due to higher risk of BIA-ALCL. Check style numbers listed to see if your implant is affected.
Allergan recalls Natrelle and McGhan 410 TruForm 2 (Soft Touch) BIOCELL breast implants (styles LL, LM, LF, ML, MM, MF, FL, FM, FF) due to higher risk of rare BIA-ALCL. This recall applies to implants used in breast augmentation or reconstruction outside the US.
Allergan recalls Natrel:150 breast implants due to higher risk of BIA-ALCL, a rare lymphoma. Affected patients should consult their doctor for evaluation.
Allergan recalls textured breast implants (Komuro, Soft Touch, BIOCELL, INTRASHIEL, BioDIMENSIONAL) linked to rare anaplastic large cell lymphoma. Affected patients should contact for evaluation.
Allergan recalls Natrelle 133 Plus tissue expanders with textured surfaces due to higher risk of anaplastic large cell lymphoma (BIA-ALCL) in some patients. Learn which models are affected and what to do.
Allergan recalls specific saline-filled breast implants due to higher risk of anaplastic large cell lymphoma (BIA-ALCL) in patients with textured implants.
