Z-1986-2021 Class II Ongoing
FDA device recall Z-1986-2021 was initiated by Philips North America Llc on May 1, 2021 and is designated Class II. Reason for recall: Significant wear of the Monitor Bracket Assembly shaft goes unrecognized could potentially lead to the Monitor Bracket Assembly detaching from the Suspension Arm and result in potential hazard for th… The recall status is ongoing. Affected quantity: 1,301 Monitor Bracket Assemblies total.
Recall Details
- Product Type
- Devices
- Report Date
- July 7, 2021
- Initiation Date
- May 1, 2021
- Termination Date
- N/A
- Voluntary/Mandated
- Voluntary: Firm initiated
- Product Quantity
- 1,301 Monitor Bracket Assemblies total
Product Description
Reason for Recall
Distribution Pattern
Worldwide distribution - US Nationwide and the countries of Canada, Mexico, AE, AR, AT, AU, BD, BE, BR, CH, CL, CN, CO, CU, CY, CZ, DE, DK, DZ, EE, EG, ES, FI, FR, GB, GE, GI, GL, GR, HK, HU, ID, IE, IL, IN, IQ, IR, IT, JO, JP, KE, KG, KH, KR, LA, LB, LK, LT, LY, MM, MN, MU, MV, MY, NI, NL, NO, NZ, OM, PA, PF, PH, PK, PL, PS, PT, QA, RE, RU, RW, SA, SE, SG , SI, SK, TH, TN, TR, UZ, VN, XK, YE, ZA, ZW.