# Pwa Industries Sdn Bhd · 80-04 · MALAYSIA — FDA import alert red lists: firms subject to detention without physical examination

For Pwa Industries Sdn Bhd · 80-04 · MALAYSIA, import alert is 80-04; import alert name is "Surveillance and Detention Without Physical Examination of Surgeon's and Patient Examination Gloves"; country is MALAYSIA; product code is 80 F - - MC Glove, Patient Examination | 80 L - - YY Glove, Patient Examination, Latex | 80 L - - YZ Glove, Patient Examination, Vinyl | 80 L - - ZA Glove, Patient Examination, Poly | 80 L - - ZC Glove, Patient Examination, Specialty; date published is 09/16/2009; address is Batu 15-1/2 , Sungai Pelong , Selangor, MALAYSIA, verified against its source on 2026-09-16.

- **Firm:** Pwa Industries Sdn Bhd _(verified: appears in the quote below)_
- **Import alert:** 80-04
- **Import alert name:** "Surveillance and Detention Without Physical Examination of Surgeon's and Patient Examination Gloves"
- **Country:** MALAYSIA _(verified: appears in the quote below)_
- **Address:** Batu 15-1/2 , Sungai Pelong , Selangor, MALAYSIA _(verified: appears in the quote below)_
- **Date published:** 09/16/2009 _(verified: appears in the quote below)_
- **Product code:** 80 F - - MC Glove, Patient Examination | 80 L - - YY Glove, Patient Examination, Latex | 80 L - - YZ Glove, Patient Examination, Vinyl | 80 L - - ZA Glove, Patient Examination, Poly | 80 L - - ZC Glove, Patient Examination, Specialty _(verified: each item appears in the quote below)_
- **Product:** A Warning Letter has been issued to this firm citing adulteration within the meaning of Section 501(h) of the Federal Food; Drug and Cosmetic Act as documented by recurring violations. Future glove shipments are subject to refusal of admission pursuant to Section 801(a)(1). Non-violative analyses may not be sufficient to remove the appearance of a violation for manufacturers/shippers Level 3 Detention. | A Warning Letter has been issued to this firm citing adulteration within the meaning of Section 501(h) of the Federal Food; Drug and Cosmetic Act as documented by recurring violations. Future glove shipments are subject to refusal of admission pursuant to Section 801(a)(1). Non-violative analyses may not be sufficient to remove the appearance of a violation for manufacturers/shippers Level 3 Detention. | A Warning Letter has been issued to this firm citing adulteration within the meaning of Section 501(h) of the Federal Food; Drug and Cosmetic Act as documented by recurring violations. Future glove shipments are subject to refusal of admission pursuant to Section 801(a)(1). Non-violative analyses may not be sufficient to remove the appearance of a violation for manufacturers/shippers Level 3 Detention. | A Warning Letter has been issued to this firm citing adulteration within the meaning of Section 501(h) of the Federal Food; Drug and Cosmetic Act as documented by recurring violations. Future glove shipments are subject to refusal of admission pursuant to Section 801(a)(1). Non-violative analyses may not be sufficient to remove the appearance of a violation for manufacturers/shippers Level 3 Detention. | A Warning Letter has been issued to this firm citing adulteration within the meaning of Section 501(h) of the Federal Food; Drug and Cosmetic Act as documented by recurring violations. Future glove shipments are subject to refusal of admission pursuant to Section 801(a)(1). Non-violative analyses may not be sufficient to remove the appearance of a violation for manufacturers/shippers Level 3 Detention. _(verified: each item appears in the quote below)_
- **FDA notes:** *** Level 3 (5/7/1999)Note | *** Level 3 (5/7/1999)Note | *** Level 3 (5/7/1999) Note | *** Level 3 (5/7/1999)Note | *** Level 3 (5/7/1999)Note _(verified: each item appears in the quote below)_

## What the source says

> Pwa Industries Sdn Bhd Date Published : 09/16/2009 Batu 15-1/2 , Sungai Pelong , Selangor, MALAYSIA 80 F - - MC Glove, Patient Examination Date Published: 09/16/2009 Desc: A Warning Letter has been issued to this firm citing adulteration within the meaning of Section 501(h) of the Federal Food; Drug and Cosmetic Act as documented by recurring violations. Future glove shipments are subject to refusal of admission pursuant to Section 801(a)(1). Non-violative analyses may not be sufficient to remove the appearance of a violation for manufacturers/shippers Level 3 Detention. Notes: *** Level 3 (5/7/1999)Note 80 L - - YY Glove, Patient Examination, Latex Date Published: 09/16/2009 Desc: A Warning Letter has been issued to this firm citing adulteration within the meaning of Section 501(h) of the Federal Food; Drug and Cosmetic Act as documented by recurring violations. Future glove shipments are subject to refusal of admission pursuant to Section 801(a)(1). Non-violative analyses may not be sufficient to remove the appearance of a violation for manufacturers/shippers Level 3 Detention. Notes: *** Level 3 (5/7/1999)Note 80 L - - YZ Glove, Patient Examination, Vinyl Date Published: 09/16/2009 Desc: A Warning Letter has been issued to this firm citing adulteration within the meaning of Section 501(h) of the Federal Food; Drug and Cosmetic Act as documented by recurring violations. Future glove shipments are subject to refusal of admission pursuant to Section 801(a)(1). Non-violative analyses may not be sufficient to remove the appearance of a violation for manufacturers/shippers Level 3 Detention. Notes: *** Level 3 (5/7/1999) Note 80 L - - ZA Glove, Patient Examination, Poly Date Published: 09/16/2009 Desc: A Warning Letter has been issued to this firm citing adulteration within the meaning of Section 501(h) of the Federal Food; Drug and Cosmetic Act as documented by recurring violations. Future glove shipments are subject to refusal of admission pursuant to Section 801(a)(1). Non-violative analyses may not be sufficient to remove the appearance of a violation for manufacturers/shippers Level 3 Detention. Notes: *** Level 3 (5/7/1999)Note 80 L - - ZC Glove, Patient Examination, Specialty Date Published: 09/16/2009 Desc: A Warning Letter has been issued to this firm citing adulteration within the meaning of Section 501(h) of the Federal Food; Drug and Cosmetic Act as documented by recurring violations. Future glove shipments are subject to refusal of admission pursuant to Section 801(a)(1). Non-violative analyses may not be sufficient to remove the appearance of a violation for manufacturers/shippers Level 3 Detention. Notes: *** Level 3 (5/7/1999)Note

## Source

- https://www.accessdata.fda.gov/cms_ia/importalert_229.html

Last verified: 2026-09-16. Review by: 2026-11-15.
Part of [FDA import alert red lists: firms subject to detention without physical examination](https://referencesource.org/fda-import-alert-red-list/).