Vehicle Safety
Recalls Search 320,000+ NHTSA safety recalls Complaints 2.1M+ consumer safety complaints TSBs 4.7M technical service bulletins VIN Lookup Decode any vehicle VIN instantly OBD Codes 12,000+ diagnostic trouble codes Fuel Economy EPA MPG data for all vehicles Statistics Recall trends & safety analysis
Consumer Safety
Product Safety 9,700+ CPSC product recalls Food Safety 28,600+ FDA food recalls Pet Safety 1.3M FDA animal adverse events Drug Safety 17,500+ FDA drug recalls Device Safety 38,400+ FDA device recalls Workplace Safety 102,900+ OSHA injury reports
Infrastructure
Bridge Safety 624,000 bridge inspections Aviation Safety 30,000+ NTSB aviation events Dam Safety 92,600 dam safety records Water Safety 433,000+ public water systems Railroad Safety 438,000+ rail crossings Pipeline Safety 8,800+ pipeline incidents
Public Health
Nursing Homes 14,700 CMS rated facilities Environmental 80,000+ hazardous sites & releases

Apollo Lap-Band AP System Small with RapidPort EZ Product Usage: The Lap-Band system consist...

FDA Device Recall #Z-2743-2018 — Class II — November 22, 2017

Recall Summary

Recall Number Z-2743-2018
Classification Class II — Moderate risk
Date Initiated November 22, 2017
Status Terminated
Voluntary Voluntary: Firm initiated

Recalling Firm

Firm Apollo Endosurgery Inc
Location West Lake Hills, TX
Product Type Devices
Quantity 54

Product Description

Apollo Lap-Band AP System Small with RapidPort EZ Product Usage: The Lap-Band system consists of a silicone band with pillows that are filled with saline and a buckle that joins the ends of the bands together, an access port and silicone tubing that connects the band to the access port. The band is placed laparoscopically around the stomach, creating a small pouch or stoma, thereby limiting food consumption. The band can be inflated or deflated with saline, through the access port, depending on patient needs and progress. The Lap-Band access port is a low-profile cylindrical port attached to kink-resistant tubing . The port is implanted subcutaneously or in the rectus muscle and can be penetrated in its silicone septum by a non-coring needle to inject or remove saline into or from the band. The kink-resistant tubing connects the access port to the band.

Reason for Recall

Component of the Lap-Band system was missing from the package

Distribution Pattern

Worldwide Distribution - FL, IL, LA, MI, MO, NC, NY, TN, TX, VA and WV and the countries of France, Italy, Spain, and United Kingdom

Lot / Code Information

Item Lot # Serial # C-2306 AF00921 S0034428 C-2306 AF00921 S0034429 C-2306 AF00921 S0034430 C-2306 AF00921 S0034431 C-2306 AF00921 S0034433 C-2306 AF00921 S0034435 C-2306 AF00921 S0034437 C-2306 AF00921 S0034439 C-2306 AF00921 S0034441 C-2306 AF00921 S0034443 C-2306 AF00921 S0034445 C-2306 AF00921 S0034447 C-2306 AF00921 S0034449 C-2306 AF00921 S0034450 C-2306 AF00921 S0034451 C-2306 AF00921 S0034453 C-2306 AF00921 S0034455 C-2306 AF00921 S0034457 C-2306 AF00921 S0034440 C-2306 AF00921 S0034433 C-2306 AF00921 S0034450 C-2306 AF00921 S0034434 C-2306 AF00921 S0034436 C-2306 AF00921 S0034438 C-2306 AF00921 S0034444 C-2306 AF00921 S0034446 C-2306 AF00921 S0034448 C-2306 AF00921 S0034452 C-2306 AF00921 S0034454 C-2306 AF00921 S0034456 C-2306 AF00921 S0034442 C-2306 AF00921 S0034432 C-20360 AF00929 S0034459 C-20360 AF00929 S0034460 C-20360 AF00929 S0034461 C-20360 AF00929 S0034463 C-20360 AF00929 S0034464 C-20360 AF00929 S0034466 C-20360 AF00929 S0034467 C-20360 AF00929 S0034468 C-20360 AF00929 S0034469 C-20360 AF00929 S0034470 C-20360 AF00929 S0034472 C-20360 AF00929 S0034473 C-20360 AF00929 S0034460 C-20360 AF00929 S0034465 C-20360 AF00929 S0034480 C-20360 AF00929 S0034486 C-20360 AF00929 S0034467 C-20360 AF00929 S0034469 C-20360 AF00929 S0034473 C-20360 AF00929 S0034458 C-20360 AF00929 S0034462 C-20360 AF00929 S0034471 C-20360 AF00929 S0034474 C-20360 AF00929 S0034475 C-20360 AF00929 S0034476 C-20360 AF00929 S0034477 C-20360 AF00929 S0034478 C-20360 AF00929 S0034479 C-20360 AF00929 S0034481 C-20360 AF00929 S0034482 C-20360 AF00929 S0034483 C-20360 AF00929 S0034484 C-20360 AF00929 S0034485 C-20360 AF00929 S0034487

Other Recalls from Apollo Endosurgery Inc

Recall # Classification Product Date
Z-2732-2014 Class II LAP-BAND AP SYSTEM AP Large with Access Port, A... Aug 15, 2014

Frequently Asked Questions

Contact your healthcare provider and the device manufacturer immediately. Check whether your specific model number and lot number are included in the recall scope. For external devices, stop using the affected product and arrange a replacement. For implanted devices, do not panic — removal is typically not required unless the risk assessment clearly indicates it. Your physician will guide you based on your individual clinical situation and the FDA's recommended actions. Report any adverse effects you may have experienced to FDA MedWatch at 1-800-FDA-1088.

Class I recalls indicate a reasonable probability of serious adverse health consequences or death from the defect. Class II recalls involve products that may cause temporary or medically reversible adverse health consequences, or where serious consequences are remote. Class III recalls cover products not likely to cause any adverse health consequences, typically involving technical regulatory violations. The classification guides urgency — Class I recalls require immediate action, while Class III may simply involve returning a product or acknowledging a labeling change. Always read the specific recall notice for recommended patient actions.

Report problems with medical devices to the FDA through MedWatch at 1-800-FDA-1088 or online at FDA.gov/safety/medwatch. Healthcare facilities are required by law to report device-related serious injuries and deaths. Patients and consumers can also report voluntarily. Include the device name, manufacturer, model number, and a description of the problem and any patient outcome. Reports from patients and clinicians help the FDA identify emerging safety signals and may trigger investigations that lead to recalls of dangerous devices.

What Should You Do?

Stop using this device if you are affected by this recall. Contact your healthcare provider and the manufacturer immediately for guidance. Report adverse events to FDA MedWatch.

More from Apollo Endosurgery Inc Recalls by Firm Recall Reasons Device Safety Stats