AmerisourceBergen PF Latex SG (Surgical Glove), Sterile, Powder Free, Size 6.5, Item No. 10112
FDA Recall Z-2036-2018 · Posted None
Advertisement
Recalling FirmWRP Asia Pacific Sdn Bhd
Recall StatusTerminated
Product CodeKGO
Date Initiated2018-05-07
Date Terminated2019-05-30
Product Quantity201,000 pairs
Reason for Recall
Some left-handed gloves contain powder. Powdered surgical gloves are a banned medical device in the U.S. Powder on natural rubber latex gloves can aerosolize latex allergens, resulting in sensitization to latex and allergic reactions. Additional risks of powdered gloves include severe airway inflammation, conjunctivitis, dyspnea, as well as granuloma and adhesion formation when exposed to internal tissue.
Firm Action
On May 7, 2018, WRP (contract manufacturer) issued an Urgent Medical Device Recall notice to its affected customer. The customer then notified its U.S. consignee, American Health Packaging, which in turn disseminated the recall information to affected consignees, down to the user level.
The following instructions were provided to affected customers:
If you are a Distributor:
1. Immediately examine your inventory, quarantine and discontinue distribution of these lots.
2. Carry out a physical count and record this data on the Business Reply Card and the Packing slip, which are included with this letter. Complete the enclosed Business Reply Card even if you do not have any product on hand.
3. Please pass this Recall Notice on ONLY to users that received these product lots.
4. Return the recalled product and the Packing Slip using the prepaid FedEx shipping labels to:
GENCO Pharmaceutical Services a subsidiary of FedEx Supply Chain
6101 North 64th Street
Milwaukee, WI 53218
If you are a User:
1. Immediately examine your inventory, quarantine and discontinue distribution of these lots.
2. If you have units of the affected products/lots in inventory, please contact GENCO Pharmaceutical Services at 877-319-8964 to receive a recall return packet. If you have not received this product you do not need to request a return packet.
3. Carry out a physical count and record this data on the Business Reply Card and the Packing slip, which are included with this letter.
4. You do not need to contact any patients.
5. Return the recalled product and the Packing Slip using the prepaid FedEx shipping labels to:
GENCO Pharmaceutical Services a subsidiary of FedEx Supply Chain
6101 North 64th Street
Milwaukee, WI 53218
To receive credit, the reply form and recalled product must be returned to GENCO by August 16th, 2018.
For questions about the recall process, call GENCO Pharmaceutical Services at (877) 319-8964.
Root Cause
Process control
Distribution Pattern
Distributors in AL, CA, OH, ID, KS, MN, NC, PA, TX.
Related FDA 510(k) Records
Devices referenced by this recall via K-numbers.
Official Source
View FDA Recall →Source: FDA Enforcement Report / Recall database. Always confirm against the official FDA record.
Advertisement